Temporomandibular Joint Disorders

30

Review clinical trials related to Temporomandibular Joint Disorders. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Calcium Gluconate Activated in Anterior Disc Displacement With Reduction of the Temporomandibular Joint

To compare the efficacy of retro discal injection of calcium gluconate-activated PRP versus non-activated PRP in adults with Anterior Disc Displacement with Reduction (ADDWR). Efficacy will be measured by the reduction of symptoms and the restoration of function, specifically targeting the normal Maximum Mouth Opening (MMO) range

Participants needed: 20
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Oct 2, 2026Locations: 1
Eligibility criteria

Adults aged 18-65 years. [+4]

• Systemic inflammatory arthritis (Rheumatoid arthritis, etc.). [+5]

Status: Not yet recruiting

Comparison of Cervical and TMJ Parameters in Young Adults With and Without Text Neck Syndrome

The aim of this cross-sectional study is to compare temporomandibular joint (TMJ) and cervical spine parameters between young university students aged 18-30 years with and without text neck syndrome, a modern overuse condition caused by prolonged digital device use and repetitive forward head flexion. Given the anatomical, biomechanical, and functional connections between the stomatognathic system and the cervical region, prolonged altered posture may contribute to TMJ dysfunction, pain, and altered physical metrics. Participants are categorized into two groups based on photographic and self-reported text neck severity (levels 3-4 for text neck vs. levels 1-2 for non-text neck) and evaluated across multiple physical parameters, including craniovertebral and cervicothoracic angles, active cervical and mandibular range of motion, cervical joint position sense, neck and TMJ pain intensity via Visual Analog Scale, TMJ dysfunction severity using the Turkish-validated Fonseca Questionnaire, static balance via the single-leg stance test, and dynamic balance via the Y Balance Test.

Participants needed: 80
Trial details
Age: 18-30Biological sex: AllType: ObservationalSponsor: Borna FarhoomandUpdated: Oct 1, 2026
Eligibility criteria

University students aged between 18 and 24 years, [+4]

History of cervical spine surgery, [+4]

Status: Recruiting

Alloplastic Total Temporomandibular Joint (TMJ) Replacement Registry

Prospective data will be collected in approximately 200 patients treated with an TMJ replacement. Patients will be followed up according to the standard (routine) for up to 5 years after the treatment. Data collection will include underlying disease, treatment details, functional and patient reported outcomes (PRO)s and anticipated or procedure-related adverse events (i.e. complications). This registry is designed to be able to assess the number of patients who refuse alloplastic total TMJ replacement. Therefore, the participating sites are asked to register all cases of refused TMJ replacements too.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: AO Innovation Translation CenterUpdated: Sep 16, 2026Locations: 23Duration: 5 Years
Eligibility criteria

Age 18 years and or older [+4]

Recent history of substance abuse (i.e. recreational drugs, alcohol) that would... [+2]

Status: Not yet recruiting

Manual Therapy vs. Home Exercise in Myogenic TMD With Neck Pain

Temporomandibular disorders (TMD) are common musculoskeletal conditions affecting the jaw joint and surrounding chewing muscles. Myogenic TMD specifically involves muscle pain and dysfunction, which is frequently accompanied by chronic neck pain due to the close anatomical and neurophysiological connections between the jaw and the cervical spine. The purpose of this study is to compare the clinical effectiveness of two widely used physiotherapy interventions-a clinician-administered manual therapy protocol and a patient-conducted home exercise program-in individuals diagnosed with myogenic TMD and chronic neck pain. The main research question is to determine whether targeted manual therapy applied to both the temporomandibular and cervical regions yields superior improvements in pain, jaw and neck mobility, quality of life, and masseter muscle properties compared to the Rocabado 6x6 home exercise program alone. 1. A total of 34 participants aged 18-45 years with myogenic TMD and chronic neck pain will be randomly allocated into two equal groups: Manual Therapy Group: Participants receive 6 individual treatment sessions (3 days per week for 2 weeks) consisting of soft tissue mobilization, trigger point therapy, myofascial release, and joint mobilization techniques applied to the jaw and neck regions. 2. Exercise Group: Participants perform the standardized Rocabado 6x6 home exercise program 3 days per week for 2 weeks, with adherence monitored through daily exercise diaries. All participants undergo comprehensive assessments at baseline and immediately following the 2-week intervention. Evaluated parameters include jaw and neck pain intensity (Visual Analog Scale), cervical and mandibular range of motion, cervical joint position sense, jaw proprioception, facial asymmetry, bruxism, TMD severity, movement-related fear (kinesiophobia), and quality of life. In addition, masseter muscle thickness and elasticity are objectively assessed using ultrasound imaging and elastography. The findings of this trial aim to provide healthcare professionals with high-level evidence regarding effective, targeted physiotherapy strategies for managing myogenic TMD co-occurring with cervical pain.

Participants needed: 34
Trial details
Age: 18-45Biological sex: AllType: InterventionalSponsor: Pamukkale UniversityUpdated: Aug 25, 2026
Eligibility criteria

Presence of TMJ pain at rest, [+3]

Any orthopedic and/or neurological condition that would preclude the assessments... [+7]

Status: Not yet recruiting

Arthrocentesis Versus Botulinum Toxin Injection in Patients With Temporomandibular Joint Disorders: A Randomized Controlled Trial

The goal of this clinical trial is to learn if arthrocentesis works as well as botulinum toxin (Botox) injection to treat pain and jaw dysfunction in adults with temporomandibular joint (TMJ) disorders. The main questions it aims to answer are: * Does arthrocentesis reduce pain more, less, or the same as Botox injection? * Does arthrocentesis improve jaw opening and function more, less, or the same as Botox injection? * What side effects do participants have with each treatment? Researchers will compare arthrocentesis to Botox injection to see which treatment works better for reducing pain and improving jaw movement in patients with TMJ disorders. Participants will: * Be randomly assigned to receive either arthrocentesis (a joint-washing procedure) or a Botox injection into the jaw muscles * Visit the clinic at 1, 3, and 6 months after treatment for checkups and assessments - Rate their pain and have their jaw movement measured at each visit * Complete short questionnaires about their jaw function and quality of life

Participants needed: 66
Trial details
Age: 18-64Biological sex: AllType: InterventionalSponsor: Mudher MB AlsunbuliUpdated: Jul 30, 2026
Eligibility criteria

Clinically and radiographically confirmed temporomandibular joint (TMJ) disorder... [+4]

Previous TMJ surgery [+6]

Status: Recruiting

ChAracterization of Normal and Pathological moRphological Variations of the TEMporomandibular Joint by Real-time magnetIc reSonance Imaging

The Real Time MRI Rapid Flash sequence is particularly interesting for the study of moving organs and joints. This sequence will make it possible to characterize normal and pathological temporomandibular joint movements by MRI.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Central Hospital, Nancy, FranceUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Adult: age ≥ 18 years old; [+3]

Person with large-scale metallic dental reconstructions; [+4]

Status: Not yet recruiting

Postoperative Assessment of Platelet-Rich Plasma and Platelet-Rich Fibrin in Temporomandibular Joint Surgery

The goal of this observational study is to evaluate postoperative outcomes following temporomandibular joint (TMJ) surgery and to compare the effectiveness of intraoperative platelet-rich plasma (PRP) and platelet-rich fibrin (PRF) injections in patients with temporomandibular joint disorders. The study includes adult patients who underwent TMJ surgery and received either PRP or PRF intraoperatively. The main questions this study aims to answer are: Whether intraoperative PRP or PRF injection is associated with differences in postoperative pain intensity and recovery. Whether PRP and PRF differ in their effects on postoperative jaw function, including maximum mouth opening and joint symptoms. If there is a comparison group: Researchers will compare patients who received intraoperative PRP with those who received intraoperative PRF to assess differences in postoperative pain, functional outcomes, and joint-related symptoms. Participants will: Have their existing medical records reviewed retrospectively. Provide postoperative outcome data derived from routine clinical follow-up, with no prospective recruitment or intervention.

Participants needed: 700
Trial details
Age: 18-75Biological sex: AllType: ObservationalSponsor: Jingping Wang, MD, Ph.D.Updated: Jun 9, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

A Combined Treatment of Manual Therapy and Nervous Vagus Stimulation in Patients With Myogenic Temporomandibular Disorders

Temporomandibular disorders (TMD) are one of the most important Public Health issues in the world and its incidence has increased over the years. The Physiotherapy and manual therapy techniques has shown its efficacy to reduce pain and to improve jaw functionality in patients with TMD. Until now, treatment targets has been the muscle and joint, but clinicians has not taken into account the innervation and how the nerve can have an influence in pain or jaw functionality. In this sense, it is known that there is a relationship between jaw innervation and vagus nerve, a parasympathetic nerve which is easily stimulable, due to its connection with the respiratory system, taking deep breaths using the diaphragm. Therefore, our hypothesis is that a treatment in which clinicians combine manual therapy and nerve vagus stimulation could have better effects (reducing pain, increasing range of motion in temporomandibular joints and improving quality of life in patients with TMD) than a isolated manual therapy treatment. With this purpose will be selected 20 subjects to participate in our study divided in two groups. Both groups will received 4 sessions of physiotherapy (one each 7 days during one month) and also will be thought to do own treatment those days the subjects does not come to the clinic until the study will have finished (the interventional period last two months). Both groups will received the same manual therapy techniques but only the experimental group will be treated with nerve vagus stimulation technique. One member of the group who will not participated in the interventions will be in charge of do evaluations (1 each month/ a total of 3 evaluations) following different questionaries to assess the primary variables of the study: chronic pain level, jaw functionality, physical symptoms level, range of motion and distress level.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of AlcalaUpdated: May 1, 2026Locations: 3
Eligibility criteria

Clinical diagnosis of myogenic pain according to the CD / TTM diagnostic criteri... [+4]

Patients with drug treatment: sedatives, anti-inflammatories, antidepressants, a... [+6]

Status: Recruiting

Effects of Focal Extracorporeal Shock Wave Therapy in the Treatment of Temporomandibular Disorders of Muscular Origin

The objective of the study is to evaluate the effectiveness of extracorporeal shock wave therapy (ESWT) in improving pain in patients with TMD pain after 5 weeks of treatment, 1 month and 3 months after the end of treatment. As secondary objectives, we plan to evaluate the effectiveness of focal shockwave therapy in relation to: 1. Range of motion (ROM) of the temporomandibular joint using goniometry after 5 weeks of treatment; 2. Degree of inflammation, using ultrasound evaluation in the temporomandibular joint relating to the degree of pain after focal shockwave therapy for 5 weeks; 3. Jaw movement (MM), joint noise (RA), joint pressure (PA) and disability index (DI) will be measured at each treatment session and after 5 weeks of treatment, 1 month and 3 months after the end of treatment in the affected joints; 4. Quality of life will be assessed using the "Short Form Health 36" questionnaire (SF-36) during the 5 weeks of treatment, 1 month and 3 months after the end of treatment; 5. Pain control medication will also be considered and compared before and after the proposed treatment for 5 weeks. Safety will be assessed throughout the study by monitoring the incidence of study-related adverse events. All patients will be contacted periodically and encouraged to report any side effects.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Sao Paulo General HospitalUpdated: Mar 25, 2026Locations: 1
Eligibility criteria

Pain in the temporomandibular region; [+5]

Abnormality in blood clotting (coagulopathy) or using some type of anticoagulant... [+15]

Status: Not yet recruiting

CBCT and Audiological Analysis of the TMJ-Tinnitus Relationship

The aim of this study is to investigate the relationship between Temporomandibular Disorders (TMD) and subjective tinnitus at both morphological and functional levels. Current literature suggests that somatosensory inputs from the temporomandibular joint (TMJ) and masticatory muscles can modulate auditory pathways, a phenomenon known as Somatosensory Tinnitus. However, the specific role of TMJ bone morphology and critical neighboring structures, such as the Petrotympanic Fissure (PTF), in this interaction remains unclear. In this clinical study, patients with tinnitus will undergo a comprehensive evaluation including Cone Beam Computed Tomography (CBCT) to quantitatively analyze condylar morphology and osteoarthritic changes. Additionally, audiological tests will be performed to assess the functional state of the auditory system. This multidisciplinary approach aims to clarify the biological link between TMD and tinnitus, potentially improving diagnostic protocols and highlighting the importance of TMJ stabilization in tinnitus management.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kutahya Health Sciences UniversityUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

Patients aged 18 years and older. [+4]

Presence of objective tinnitus (e.g., vascular or muscular origin). [+6]

Status: Not yet recruiting

Cross Cultural Adaptation, Reliability &Validity of The Arabic Version of 8_Item Jaw Functional Limitation Scale In Temporomandibular Joint Disorders

The purpose of this study is to test if the translated Arabic version of the (jaw functional limitation scale -8) JFLS\_8 , valid (face, content, feasibility) ,reliable (internal consistency, test retest) and culturally adapted enough to quantify the impact of temporomandibular joint (TMJ) disorders on jow function in arabic people or not?

Participants needed: 100
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Mar 4, 2026Locations: 1
Eligibility criteria

Patients aged 18 to 65 years . [+4]

History of trauma (recent head or neck or TMJ severe trauma) [+2]

Status: Recruiting

The Effect of Body Awareness Therapy on Pain, Function and Psychosocial Parameters in Temporomandibular Joint Disorders

This randomized, single-blind controlled trial aims to investigate the effectiveness of Body Awareness Therapy (BAT) on pain, functional limitations, and psychosocial outcomes in individuals with temporomandibular joint disorders (TMD). TMD is characterized by orofacial pain, impaired jaw function, and increased psychosocial burden, yet current physiotherapy approaches may not fully address the biopsychosocial mechanisms underlying these symptoms. BAT is a structured mind-body physiotherapy intervention designed to improve postural awareness, interoceptive sensitivity, breathing regulation, and movement control. In this study, participants will be randomly assigned to either BAT or a standard physiotherapy control intervention for a defined treatment period. Primary outcomes will include pain intensity and jaw functional limitations, while secondary outcomes will assess body awareness, anxiety, stress, and quality of life. Evaluations will be conducted at baseline and post-intervention. The findings of this trial may provide evidence for integrating biopsychosocial and awareness-based physiotherapy into TMD rehabilitation.

Participants needed: 52
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Recep Tayyip Erdogan UniversityUpdated: Feb 3, 2026Locations: 1
Eligibility criteria

Not listed

Status: Not yet recruiting

Temporomandibular Joints Mobility and Head Posture: Influence of Manual Therapy and Exercises in Dental Patients.

Goal: This clinical study aims to investigate how the range of motion of the temporomandibular joints (TMJ) changes in relation to the patient's head posture. Furthermore, we will assess the efficacy of a specific physiotherapy program in improving TMJ mobility and influencing head alignment in patients undergoing orthodontic treatment or prosthetic reconstruction. Scope: The project will evaluate TMJ function and head alignment in orthodontic or prosthetic patients aged 11-65. The core focus is to analyze the correlation between head posture and TMJ mobility and to measure changes in these parameters before and after the manual physiotherapy intervention.

Participants needed: 100
Trial details
Age: 11-65Biological sex: AllType: InterventionalSponsor: The Jerzy Kukuczka Academy of Physical Education in KatowiceUpdated: Dec 22, 2025
Eligibility criteria

Patients aged 11 to 13 years with a confirmed occlusion class (Class I, II, or I... [+2]

Inability to perform required study tests or procedures. [+8]

Status: Recruiting

Clinical Validation of DystoniaNet Deep Learning Platform for Diagnosis of Isolated Dystonia

This research involves retrospective and prospective studies for clinical validation of a DystoniaNet deep learning platform for the diagnosis of isolated dystonia.

Participants needed: 1,000
Trial details
Biological sex: AllType: InterventionalSponsor: Massachusetts Eye and Ear InfirmaryUpdated: Dec 2, 2025Locations: 1
Eligibility criteria

Males and females of diverse racial and ethnic backgrounds, with age across the... [+2]

Patients who are incapable of giving informed consent; [+1]

Status: Recruiting

Assessing Symptom and Mood Dynamics in Pain Using the Smartphone Application SOMA

This study relies on the use of a smartphone application (SOMA) that the investigators developed for tracking daily mood, pain, and activity status in acute pain, chronic pain, and healthy controls over four months.The primary goal of the study is to use fluctuations in daily self-reported symptoms to identify computational predictors of acute-chronic pain transition, pain recovery, and/or chronic pain maintenance or flareups. The general study will include anyone with current acute or chronic pain, while a smaller sub-study will use a subset of patients from the chronic pain group who have been diagnosed with chronic low back pain, failed back surgery syndrome, or fibromyalgia. These sub-study participants will first take part in one in-person EEG testing session while completing simple interoception and reinforcement learning tasks and then begin daily use of the SOMA app. Electrophysiologic and behavioral data from the EEG testing session will be used to determine predictors of treatment response in the sub-study.

Participants needed: 800
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Brown UniversityUpdated: Sep 19, 2025Locations: 1
Eligibility criteria

Age above 18 [+23]

recent injury or surgery unrelated to the pain in the past 3 months [+20]

Status: Not yet recruiting

Post-Isometric Relaxation in Temporomandibular Disorders

This planned randomized, single-blind clinical trial will investigate the effects of adding the Post-Isometric Relaxation (PIR) technique to a standard postural exercise program in individuals with moderate to severe temporomandibular joint dysfunction (TMD). Forty volunteers aged 18-25 years will be recruited and randomly assigned to either an experimental group (postural exercises + PIR) or a control group (postural exercises only). The intervention will be delivered three times per week for six weeks. Primary outcomes will include cervical range of motion, mandibular mobility, head anterior tilt, and thoracic kyphosis index, measured before and after the intervention. The study aims to determine whether PIR provides additional benefits to standard postural exercises in improving jaw and neck function and postural alignment in young adults with TMD.

Participants needed: 40
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Sanem ŞENERUpdated: Aug 19, 2025
Eligibility criteria

Age between 18 and 25 years [+6]

History of jaw or facial trauma within the past year [+6]

Status: Not yet recruiting

Evaluation of the Effect of Laser Therapy on Lateral Pterygoid Muscle in Patients With Wilke's Stage I and II Temporomandibular Disorders (TMD): Case Series Study

The purpose of this study will be to evaluate the effect of laser therapy on lateral pterygoid muscle in patients with Wilke's stage I and II temporomandibular disorders (TMD).

Participants needed: 25
Trial details
Age: 16-50Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jun 13, 2025
Eligibility criteria

Patients age between 16-50 years with no sex predilection. [+3]

Patients with previous temporo-mandibular surgeries. [+3]

Status: Not yet recruiting

Patient Satisfaction in Occlusal Splints Fabricated Using Fully Digital Versus Conventional Workflow

According to published literatures, the prevalence of TMD is approximately 10% in patients over 18 years of age with a considerable proportion being women of reproductive age. The treatment of TMD presents the following goals: decreasing joint and masticatory muscle pain, increasing the range of motion in the mandible, preventing degenerative changes in the articulating tissues. Management of TMD can be either conservative or surgical treatments, the conservative treatments include analgesia, medications, physical therapy, occlusal adjustment, splint therapy, localized steam application, and external muscle massage. The occlusal splint therapy is considered a common treatment option for TMD management. Flat stabilization splint is the preferred splint for such cases. It is designed to promote occlusal stability and decrease muscles tension by altering occlusion and allowing complete seating of the condyle in centric relation. The evolution of digital technology created new era of dentistry that successfully digitalized the traditional workflow of occlusal splints including designing and manufacturing. Furthermore, virtual facebow and dynamic jaw relation record using jaw tracking device are another digital reward. The digital workflow can offer more predictable approach for occlusal splint construction, It could eliminate the traditional technical errors and enhance the occlusal accuracy

Participants needed: 32
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: May 22, 2025
Eligibility criteria

18-40 years old [+6]

Patients with systemic diseases which could affect TMJ, e.g., rheumatoid arthrit... [+5]

Status: Not yet recruiting

Long-term Safety and Performance of Materialise's Patient-specific TMJ System.

This is a long-term (10 years), retrospective-prospective, observational, single-arm, monocenter study of patients to be treated with the Materialise TMJ Total Arthroplasty System for TMJ replacement. The study will evaluate the efficiency, safety, clinical performance, accuracy, benefits, and risks associated with long-term use and the impact on life quality and diet of the TMJ system, its fixation devices, TMJ Implant trial, and guides in the adolescent and adult populations.

Participants needed: 30
Trial details
Biological sex: AllType: ObservationalSponsor: MaterialiseUpdated: Apr 30, 2025Locations: 1
Eligibility criteria

Patients prescribed with Materialise TMJ Total Arthroplasty System for TMJ recon... [+1]

Known hypersensitivity to Titanium, Nickel, or Cobalt-Chrome alloys. [+5]

Status: Recruiting

Cognitive Exercise Therapy Approach Biopsychosocial Questionnaire (BETY-BQ) in Patient with Temporomandibular Disorders

The aim of this study is to investigate the validity, reliability, and responsiveness of the Cognitive Exercise Therapy Approach-Biopsychosocial Questionnaire (BETY-BQ) in individuals with temporomandibular disorder. The following are alternative hypotheses of the study: * BETY-BQ has significant convergence with the Patient Health Questionnaire-9 measuring depression. * BETY-BQ has significant convergence with the Patient Health Questionnaire-15 measuring physical symptoms. * BETY-BQ has significant convergence with the Generalized Anxiety Disorder-7 measuring anxiety. * BETY-BQ has significant convergence with the Short Form-36 measuring quality of life. * BETY-BQ has significant convergence with the Craniomandibular Pain and Disability Inventory measuring disability. * BETY-BQ has significant convergence with the Mandibular Function Impairment Questionnaire measuring function. * BETY-BQ has significant stability. * BETY-BQ has significant internal consistency.

Participants needed: 150
Trial details
Age: 18-64Biological sex: AllType: ObservationalSponsor: Hacettepe UniversityUpdated: Mar 13, 2025Locations: 2
Eligibility criteria

Having received a diagnosis of temporomandibular disorder

Experiencing difficulty in cooperating to fill out the questionnaires [+1]

Status: Recruiting

Tele-Rehabilitation in Patients With Temporomandibular Dysfunction

Temporomandibular disorder or TMD is characterized by a set of symptoms such as: pain, decreased range of motion and joint noise. It's origin is multifactorial, which may be related to biological aspects, environmental and psychosocial. The multimodal approach has been widely used in physiotherapy for the treatment of TMDs. Physiotherapy has been walking together with technology so that telerehabilitation can be a reality, contributing so that quality care reaches the patient, in the impossibility office-to-face service. The objective of this study is to verify the effect of telerehabilitation on pain outcomes, range of motion, functionality and biopsychosocial aspects in individuals with temporomandibular disorders. Will be a randomized, controlled and blinded clinical trial was carried out. The study will be divided into two moments: evaluation and intervention. Evaluations will be carried out using the Diagnostic Criteria for Temporomandibular Disorders: Clinical Protocol and Assessment Instruments (DC/TMD), the Fonseca Anamnesis Index (IAF), the Numerical Pain Scale (END) and the Functional Limitation Questionnaire (MFIQ). Individuals will be randomized into 2 groups: Group A (in person) Group B (telerehabilitation). Both groups will receive treatment physical therapy for 12 weeks. After collecting the data, they will be tabulated and analyzed using a 5% significance level.

Participants needed: 50
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: University of Nove de JulhoUpdated: Mar 4, 2025Locations: 1
Eligibility criteria

Age between 18 and 60 years; [+2]

Status: Recruiting

Efficacy of Repetitive Transcranial Magnetic Stimulation in Temporomandibular Disorders.

Temporomandibular disorder (TMD) refers to a group of musculoskeletal conditions that affect the temporomandibular joint (TMJ), the masticatory muscles, and the associated structures. It is assumed that 30 to 40% of cases of acute painful TMD becomes chronic. Chronic pain is a significant public health problem, affecting professional and social activities, emotional state, and quality of life. The pathophysiological mechanisms involved in chronic orofacial pain are complex and multifaceted and not yet fully understood. The coexistence of psychological factors associated with vast peripheral and central mechanisms makes chronic orofacial pain treatment a complex challenge. Due to the complexity of chronic TMDs, some patients remain refractory to current therapeutic methods. Thus, several efforts have been made to develop therapies aimed at the treatment of neuroplastic changes induced by chronic pain. In this sense, transcranial stimulation methods appear to be a promising technique. Transcranial Magnetic Stimulation (TMS) is a non-invasive, safe, and approved treatment for clinical use in psychiatric disorders such as depression and chronic pain. Given the above, it is necessary to develop studies to investigate the TMS effectiveness in chronic TMD. This study aims to evaluate the effectiveness of transcranial magnetic stimulation in patients with chronic temporomandibular disorders. An additional objective is to determine possible predictors for treatment success based on the assessment of functional brain connectivity and psychosocial characteristics.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of CoimbraUpdated: Feb 13, 2025Locations: 1
Eligibility criteria

Individuals of both sexes, literate, aged over 18 years with the diagnosis of mu... [+2]

Volunteers who present verbal communication impairment due to a neurological dis... [+3]

Status: Recruiting

Internal Photobiomodulation For Management Of Temporomandibular Joint Internal Derangement

Aim of the study was to compare the efficacy of internal versus external photobiomodulation (PBM) in the management of patients with TMJ internal derangements (TMJ-ID).

Participants needed: 50
Trial details
Age: 20-40Biological sex: AllType: InterventionalSponsor: Nourhan M.AlyUpdated: Jan 8, 2025Locations: 1
Eligibility criteria

Painful click at temporomandibular joint (TMJ) area. [+2]

Patients who have radiographic evidence of degenerative conditions of TMJ. [+5]

Status: Recruiting

Balance, TMJ, Social Adaptive Assessment in Individuals With Autism Spectrum Disorder

The aim of our study is to evaluate temporomandibular joint (TMJ), cervical posture, balance, dual-task performance, and social adaptation skills in individuals with autism. The study will be conducted at Bartın Lider Special Education and Rehabilitation Center following the approval of the ethics committee. Individuals determined by the sample size calculated through power analysis will be included in the study. First, the socio-demographic characteristics (age, height, body weight, body mass index, education level, exercise and smoking habits, etc.) of the participants who voluntarily join the study will be recorded. Participants will be divided into two groups: individuals with typical motor development and those with autism spectrum disorder (ASD), and the same assessment tools will be used for both groups. Individuals with typical motor development will serve as the control group. The assessment tools include the Timed Up and Go (TUG) test, the 10-Meter Walk Test, the Vineland Adaptive Behavior Scale, the PostureScreen Android-based posture assessment application, and the Helkimo Clinical Dysfunction Index for craniomandibular disorders. Based on the evaluation results, the relationships between TMJ, cervical posture, functional balance, dual-task performance, and social adaptation skills in individuals with autism will be analyzed and compared with those of individuals with typical motor development.

Participants needed: 23
Trial details
Age: 4-21Biological sex: AllType: ObservationalSponsor: Kırıkkale UniversityUpdated: Dec 6, 2024Locations: 1
Eligibility criteria

Having a diagnosis of Autism Spectrum Disorder (ASD) confirmed by a physician. [+5]

Individuals with comorbid secondary health conditions. [+1]

Status: Recruiting

Temporomandibular Disorder in Use of Levonorgestrel Intrauterine System

The goal of this clinical trial is to investigate the possible role of levonorgestrel intrauterine system use(LIU) in the pathogenesis of temporomandibular joint disorder (TMD). In this clinical trial, levonorgestrel intrauterine system patients (n=30) aged 25-50 and control group patients (n=30) with the same demographics and age range are used. The main questions it aims to answer are: To compare the frequency of temporomandibular dysfunction in women using the levonorgestrel intrauterine system with the control group of the same demographic and age range. The levonorgestrel intrauterine system use group consisted of 50 women who had previously a mirena implanted by a gynecologist at least 3 months ago due to menstrual bleeding and pelvic pain. The control group included 50 randomised healthy women who had regular menstrual cycles and were not taking any medication.

Participants needed: 100
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Marmara UniversityUpdated: Nov 25, 2024Locations: 1
Eligibility criteria

Being a woman [+3]

Patients with craniofacial syndrome [+5]