Clinical trials

30

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Condition / disease
Location
Status: Not yet recruiting

CBT-Based Stress Management Program for Healthcare Students

This study aims to evaluate the effectiveness of a cognitive-behavioral-based stress management skills program for healthcare students. The study will use a mixed-methods design and will include intervention, placebo, and control groups. Approximately 90 healthcare students will participate in the experimental phase. The intervention group will receive a 9-session cognitive-behavioral-based stress management program designed to help students recognize and manage stress, identify dysfunctional thoughts, and develop effective stress management and coping skills. The study will assess changes in perceived stress and coping skills before and after the program and at follow-up. Qualitative interviews and group discussions will also be conducted to explore students' experiences and perceptions of stress management and the program. It is hypothesized that students who participate in the stress management program will show improvements in perceived stress and coping skills compared with students in the placebo and control groups.

Participants needed: 90
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Oct 1, 2026Locations: 1
Eligibility criteria

Be an active student in an associate or undergraduate program at the university. [+5]

Have a history of a psychiatric diagnosis (e.g., major depressive disorder, bipo... [+6]

Status: Recruiting

Effect of Local Anesthesia Techniques on Pulp Hemostasis in Primary Molars

The goal of this clinical trial is to compare the effects of two local anesthesia techniques on pulp hemostasis time during pulpotomy treatment of mandibular primary molars in children aged 6-9 years. The main questions it aims to answer are: Does the local anesthesia technique affect the time required to achieve pulp hemostasis during pulpotomy? Are there differences between the two anesthesia techniques in terms of pain, heart rate, and oxygen saturation during treatment? Researchers will compare conventional inferior alveolar nerve block anesthesia with computer-controlled intraosseous local anesthesia using the QuickSleeper 5 system to determine whether the anesthesia technique affects pulp hemostasis time and the secondary clinical outcomes. Each participant will receive both anesthesia techniques in a randomized order using a split-mouth design. Participants will: Receive conventional inferior alveolar nerve block anesthesia for pulpotomy treatment of one mandibular primary molar. Receive computer-controlled intraosseous local anesthesia using the QuickSleeper 5 system for pulpotomy treatment of the contralateral mandibular primary molar at a separate treatment session. Have pulp hemostasis time recorded during each pulpotomy procedure. Have pain, heart rate, and oxygen saturation assessed during the treatment procedures.

Participants needed: 40
Trial details
Age: 6-9Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Sep 14, 2026Locations: 1
Eligibility criteria

Children aged 6-9 years. [+7]

Children with systemic health conditions classified as ASA physical status III o... [+6]

Status: Not yet recruiting

Effect of Guided Imagery on Sleep Quality, State Anxiety, and Comfort in Patients With Acute Coronary Syndrome

The goal of this randomized controlled trial is to determine whether guided imagery, when added to routine care, can reduce state anxiety and improve sleep quality and comfort in adults with acute coronary syndrome who are being treated in a cardiac intensive care unit. The main questions this study aims to answer are: Does guided imagery reduce state anxiety compared with routine care alone? Does guided imagery improve sleep quality compared with routine care alone? Does guided imagery improve comfort compared with routine care alone? A total of 64 participants will be randomly assigned to either a guided imagery group or a routine care group using block randomization. Participants in the guided imagery group will receive routine care and listen to a standardized guided imagery audio recording through headphones twice a day for two consecutive days. Each guided imagery session will last approximately 15 minutes. Participants in the routine care group will receive the standard treatment and nursing care provided in the cardiac intensive care unit without guided imagery. Researchers will assess participants' anxiety, sleep quality, and comfort and compare the changes between the two groups.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Aug 31, 2026
Eligibility criteria

Age 18 years or older. [+9]

Diagnosis of unstable angina pectoris. [+10]

Status: Recruiting

Reliability and Validity of Three DT-TUG Protocols in MS

Dual-tasking is performing two different tasks at the same time. For example, singing while cooking. Everyday activities often involve dual-task. In many researches evaluating dual-task performance in individuals with MS, it has been reported that individuals with severe disability, in particular, exhibit greater effort than healthy individuals. This increase in motor and cognitive dual-task performance in individuals with Multiple Sclerosis (MS) is associated with an increased risk of falls. There is a need for standardized, valid, and reliable assessment tools to evaluate dual-task performance in MS. The purpose of this study is to examine and compare the validity and reliability of the dual-task Timed Up and Go test administered using three different protocols.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Aug 27, 2026Locations: 1
Eligibility criteria

Having been diagnosed with MS according to the McDonald criteria revised in 2017... [+3]

Pregnancy; [+4]

Status: Not yet recruiting

Digital Health Literacy and Social Participation in Individuals With Hemiplegia

This cross-sectional observational study aims to investigate the association between digital health literacy and social participation in individuals with hemiplegia after stroke. A total of 250 adults with a history of stroke at least 6 months previously will be included. Digital health literacy will be assessed using the eHealth Literacy Scale (eHEALS), and social participation will be assessed using the Reintegration to Normal Living Index (RNLI). The secondary aim is to examine the associations of digital health literacy with anxiety and depression, functional independence, and fatigue.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Aug 19, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Not listed

Status: Recruiting

Relationship Between Single- and Dual-Task Obstacle Crossing Performance and Fatigue and Disability in Multiple Sclerosis

This cross-sectional observational study aims to investigate the relationship between obstacle crossing performance under single-task and dual-task conditions and the levels of fatigue and disability in individuals with Relapsing-Remitting Multiple Sclerosis (RRMS). Walking performance will be assessed under standard walking and obstacle crossing conditions with and without a concurrent cognitive task. The study will examine how increased task complexity affects walking performance and its association with fatigue, disability, cognition, and functional mobility.

Participants needed: 30
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jul 31, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Age between 18 and 65 years. [+7]

Multiple sclerosis relapse within the previous month. [+3]

Status: Not yet recruiting

Salivary Cytokines, MMP-8 and Dental Caries in Osteoporosis Patients

This study examines saliva samples from patients with osteoporosis. The levels of cytokines and Matrix Metalloproteinase-8 (MMP-8) enzyme in saliva will be measured. Additionally, the dental caries status of participants will be evaluated. The aim of this study is to understand the relationship between osteoporosis and oral health. Only saliva samples will be collected from participants; no treatment or medication will be administered.

Participants needed: 50
Trial details
Age: 45-75Biological sex: AllType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jul 16, 2026
Eligibility criteria

Willing to give voluntary consent For Group 1, having been diagnosed with osteop...

Having a chronic inflammatory or autoimmune disease Using glucocorticoids, anti-...

Status: Not yet recruiting

Pain After Diode Laser Frenectomy in Children

This prospective single-group clinical study aims to evaluate postoperative pain following diode laser-assisted frenectomy in pediatric patients and to assess the agreement between different pediatric pain assessment scales. Children aged 8 to 14 years who require diode laser-assisted frenectomy will be treated according to the standard clinical protocol at the Pediatric Dentistry Clinic of Afyonkarahisar Health Sciences University. Postoperative pain will be evaluated once daily for seven consecutive days using the Wong-Baker FACES Pain Rating Scale, the Modified Emoji Pain Scale (MEPS), and gender-specific pain assessment scales. The primary objective is to characterize the time course of postoperative pain during the first postoperative week. Secondary objectives include evaluating the agreement and correlation between the different pain assessment instruments used in pediatric patients. The findings are expected to contribute to the identification of reliable pain assessment methods and to improve postoperative pain evaluation following diode laser-assisted frenectomy in children.

Participants needed: 53
Trial details
Age: 8-14Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jul 15, 2026Locations: 1
Eligibility criteria

Children aged 8 to 14 years. [+4]

Presence of systemic diseases or medical conditions that could influence wound h... [+6]

Status: Recruiting

Repetitive Transcranial Magnetic Stimulation in Cardiac Autonomic Dysfunction

The aim of this study is to investigate the effects of repetitive transcranial magnetic stimulation (rTMS) added to conventional neurological rehabilitation on heart rate variability (HRV), quality of life, upper extremity muscle strength and autonomic symptoms in patients with stroke.

Participants needed: 44
Trial details
Age: 35-80Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Participants aged 35-80 years admitted to the Afyonkarahisar Health Sciences Uni... [+3]

Serious cardiac disease, uncontrolled hypertension [+11]

Status: Recruiting

Repetitive Transcranial Magnetic Stimulation Therapy in Spinal Cord Injury Related Neuropathic Pain

The aim of our study is to investigate the effect of different protocols of high-frequency Repetitive Transcranial Magnetic Stimulation (rTMS) therapy added to the rehabilitation program on neuropathic pain,depression, quality of life and quality of sleep compared to each other and placebo group in participants with spinal cord injury.

Participants needed: 63
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Having an important comorbid disease such as severe heart disease (aortic stenos... [+14]

Status: Not yet recruiting

Game-Based Handwashing Education in Preschool Children

This study aims to evaluate the effect of a game-based handwashing education program, which will be developed based on the Health Belief Model, on the handwashing behaviors of preschool children. Preschool children are considered more vulnerable to respiratory and gastrointestinal infections due to their immature immune systems and close contact with peers in school settings. Within the scope of this project, a game called "Clean Hands" will be developed and a game-based handwashing education program will be implemented. The study will be conducted using a quasi-experimental pretest-posttest control group design with children aged 60-83 months attending two preschools with similar demographic characteristics. Children will be assigned to intervention and control groups. Children in the intervention group will participate in the developed game as a group activity once a week for eight weeks. The control group will not receive any game-based intervention during the study period; however, the same game will be provided to the control group after completion of the intervention sessions. Data will be collected using teacher observation forms, parent observation forms, handwashing step sequencing assessment forms, and handwashing behavior discrimination assessment forms. The findings are expected to contribute to the development of effective game-based health education strategies for preschool children.

Participants needed: 108
Trial details
Age: 60-83Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: May 26, 2026
Eligibility criteria

Participation in at least 80% of the planned 8 game sessions (at least 7 session... [+4]

Children outside the 60-83 months age range [+4]

Status: Recruiting

Comparison of Ultrasound-Guided Injection With Median Nerve Decompression Surgery in Carpal Tunnel Syndrome

The aim of this study is to compare ultrasound-guided perineural injection of the median nerve with classic minimal incision surgical technique for median nerve decompression in patients diagnosed with mild, moderate, and severe carpal tunnel syndrome.

Participants needed: 60
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 12, 2026Locations: 1
Eligibility criteria

The presence of symptoms such as nocturnal, posture-related, or movement-related... [+3]

Individuals who may exhibit symptoms mimicking carpal tunnel syndrome, such as c... [+8]

Status: Recruiting

The Relationship Between Ultrasonographic Findings and Sleep Quality in Carpal Tunnel Syndrome

The aim of our study is to determine the relationship between disease severity and sleep quality in CTS patients and to compare the findings with healthy controls.

Participants needed: 120
Trial details
Age: 20-80Biological sex: AllType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Patients diagnosed with CTS according to the criteria of the American Academy of...

Patients with radiculopathy, brachial plexopathy, thoracic outlet syndrome and t... [+7]

Status: Recruiting

Transcranial Magnetic Stimulation Therapy in Neuropathic Painful Spinal Cord Injury Patients

The aim of our study is to investigate the effect of high-frequency Repetitive Transcranial Magnetic Stimulation(rTMS) therapy applied to the dorsolateral PFC (DLPFC) area on neuropathic pain in patients with spinal cord injury. In this area, there are very few studies on the effectiveness of rTMS treatment added to medical treatment in neuropathic pain. In addition, the number of studies comparing the effect of rTMS therapy applied to the DLFPC area is very few.

Participants needed: 60
Trial details
Age: 20-70Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 9, 2026Locations: 1
Eligibility criteria

Having spinal cord injury with neurophatic pain at least six months ago, [+3]

Epilepsy, [+12]

Status: Not yet recruiting

Effect of Play Dough, Slime, and Plush Toys on Dental Anxiety and Pain in Children During Dental Treatment

This study aims to evaluate the effectiveness of tactile distraction materials, including play dough, slime, and plush toys, on dental anxiety, pain perception, and physiological stress responses in children undergoing dental treatment. Ninety children aged 6-10 years receiving restorative dental treatment under local anesthesia were randomly assigned to one of four groups: play dough, slime, plush toy, or control group without distraction. Dental anxiety and pain levels were assessed using validated psychometric scales, while physiological stress responses were evaluated through heart rate monitoring and salivary cortisol measurements. The study seeks to determine whether simple non-pharmacological distraction techniques can improve behavioral cooperation and reduce anxiety and pain perception during pediatric dental procedures. Findings may contribute to the development of child-friendly dental management strategies and enhance the quality of pediatric dental care.

Participants needed: 90
Trial details
Age: 6-10Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 3, 2026
Eligibility criteria

Children aged 6-10 years requiring restorative dental treatment. [+5]

Presence of systemic diseases or medical conditions affecting stress response or... [+5]

Status: Not yet recruiting

DETERMINATION OF THE EFFECTS OF STAINLESS STEEL CROWNS CEMENTED WITH RESIN CEMENTS ON INTERLEUKIN-10, 12, 18 LEVELS IN GINGIVAL CREVICULAR FLUID

This split-mouth clinical study aimed to evaluate the early effects of stainless steel crowns cemented with self-adhesive resin cement and high-viscosity glass ionomer cement on clinical periodontal parameters and interleukin-10 (IL-10), interleukin-12 (IL-12), and interleukin-18 (IL-18) levels in gingival crevicular fluid in pediatric patients. The study included 45 systemically healthy children aged 6-10 years. Stainless steel crowns were placed on the mandibular second primary molars (teeth 75 and 85) in each patient; tooth 75 was cemented with a self-adhesive resin cement (G-Cem ONE™, GC, Japan), while tooth 85 was cemented using a high-viscosity glass ionomer restorative material (EQUIA Forte™ HT, GC, Tokyo, Japan). Plaque index, gingival index, and bleeding on probing were recorded before treatment and one week after cementation. Gingival crevicular fluid samples were collected at the same time points, and IL-10, IL-12, and IL-18 levels were analyzed using the ELISA method. A statistically significant reduction in plaque index values was observed in both cement groups at the one-week follow-up (p\<0.001), whereas no significant differences were found in gingival index or bleeding on probing values (p\>0.05). IL-10 and IL-12 levels did not change significantly in either group, whereas IL-18 levels decreased significantly in the resin cement group and were significantly higher in the glass ionomer cement group postoperatively. These findings suggest that although different cementation materials used for stainless steel crowns yield similar short-term clinical periodontal outcomes, material-related differences may exist in gingival biological responses, particularly with respect to IL-18 levels.

Participants needed: 45
Trial details
Age: 6-10Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Feb 19, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Physiological and Biochemical Responses to Blood Flow Restriction Training

This study is designed to examine the short-term and long-term effects of blood flow restriction exercise training on physiological and biochemical markers in individuals who are new to strength training and in experienced athletes training at different load levels. This exercise method involves placing a special inflatable cuff around the upper part of the thigh. The cuff partially limits blood flow to the area, which helps the muscles work more effectively during exercise. The cuff will be applied only to the individual's dominant leg (the leg you use more often in daily activities), but all exercises will be performed using both legs. The exercise program will last for a total of six weeks and will be carried out twice per week. The pressure applied by the cuff will be individually adjusted based on each participant's physical characteristics to ensure safety and comfort. The study will include a total of 30 healthy participants aged between 18 and 40 years. Participants will be divided into two groups: individuals who have recently started strength training and experienced athletes with different levels of training experience.

Participants needed: 30
Trial details
Age: 18-40Biological sex: MaleType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Feb 13, 2026Locations: 1
Eligibility criteria

Voluntary participation of healthy adults [+4]

History of hypertension, cardiovascular diseases, peripheral vascular diseases,... [+2]

Status: Recruiting

Comparison of Rest Splints vs High-Intensity Laser Therapy in Carpal Tunnel Syndrome

The aim of this study is to compare the effectiveness of rest splints and high-intensity laser therapy(HILT) added to physical therapy programs for patients with carpal tunnel syndrome in terms of pain, function, nerve conduction studies, and grip strength.

Participants needed: 78
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jan 13, 2026Locations: 2
Eligibility criteria

Patients aged 18-75 years who have been diagnosed with carpal tunnel syndrome ba...

Diabetes Mellitus [+14]

Status: Recruiting

Validity and Reliability of the PRAFAB

PRAFAB assesses both the objective and subjective aspects of urinary incontinence. While differing from other questionnaires in this respect, it consists of only five questions. Today, there is a need for multidimensional and easy-to-use scales that can assess the effects of incontinence on quality of life. Therefore, the aim of this study is to conduct a Turkish validity and reliability study of the PRAFAB questionnaire in women with urinary incontinence.

Participants needed: 63
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jan 14, 2026Locations: 1
Eligibility criteria

Being 18 years of age or older [+2]

Being pregnant, [+2]

Status: Not yet recruiting

The Effect of Art-Based Mandala Coloring Activity on Postpartum Anxiety and Postpartum Depression

The postpartum period is a critical time for women's physical and psychological health, during which significant hormonal, emotional, and social changes occur. During this period, many women experience increased stress, anxiety, and emotional vulnerability while adapting to new parental responsibilities and caring for a newborn. When these challenges are not adequately managed, they may contribute to the development of postpartum anxiety and postpartum depression, which can negatively affect maternal well-being, mother-infant bonding, breastfeeding practices, and child development. Despite the importance of postpartum mental health, non-pharmacological and easily accessible supportive interventions remain limited. This randomized controlled experimental study aims to evaluate the effect of a structured, art-based mandala coloring activity on postpartum anxiety and postpartum depression among postpartum women. The study will be conducted at Afyonkarahisar Health Sciences University Health Practice and Research Center, Obstetrics and Gynecology Clinic, and will include women who have recently given birth at this institution. Eligible participants will be randomly assigned to either an intervention group or a control group. Women in the intervention group will receive individual training in mandala coloring before hospital discharge and will be provided with mandala coloring materials for home use. They will be encouraged to engage in the mandala coloring activity over an eight-week period and will be followed through regular telephone contacts. In addition to monitoring participation in the activity, individualized supportive counseling will be provided based on participants' needs. Women in the control group will receive routine postpartum care without any additional intervention. Postpartum anxiety and postpartum depression levels will be assessed at multiple time points during the study to examine changes over time. This study seeks to determine whether mandala coloring, as a low-cost and non-pharmacological art-based activity, may serve as a supportive approach to improve psychological well-being during the postpartum period. The findings may contribute to the development of accessible interventions aimed at supporting maternal mental health in the early postpartum period.

Participants needed: 60
Trial details
Age: 18-49Biological sex: FemaleType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jan 7, 2026
Eligibility criteria

Able to speak and understand Turkish [+7]

Have previously received psychological or psychiatric treatment or are receiving... [+7]

Status: Recruiting

Effects of Adding Balneotherapy to a Physical Therapy Program in Patients With Chronic Lumbar Radiculopathy

The aim of this study is to investigate the effects of adding balneotherapy to the conventional physical therapy program on neuropathic pain, disability, daily living activities, and sleep quality in patients with chronic lumbar radiculopathy.

Participants needed: 120
Trial details
Age: 18-75Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Mar 21, 2025Locations: 2
Eligibility criteria

Patients aged between 18 and 75 years who have been diagnosed with chronic lumba...

Patients with thermoregulation disorders or sensory deficits [+30]

Status: Not yet recruiting

Effect of Music During Wound Debridement

This randomized controlled intervention study aims to investigate the effect of music played before the debridement on patients' anxiety, pain, and sense of safety. The study will be carried out with two groups: The control and the intervention groups with 100 participants for each group. While the control group participants will receive standard care, the intervention group participants will listen to selection of Sufi music before the debridement in addition to standard care.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Feb 19, 2025
Eligibility criteria

18 years of age or above, [+7]

Patients under 18 years of age, [+7]

Status: Not yet recruiting

Effect of Music During Toe Amputation

This randomized controlled intervention study aims to investigate the impact of music played during toe amputation on patients' anxiety, pain, sense of safety, and fear of surgery. The study will be carried out with two groups: The control and the intervention groups with 60 participants for each group. While the control group participants will receive standard care, the intervention group participants will listen to selection of Sufi music during the whole amputation procedure in addition to standard care.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Feb 11, 2025Locations: 1
Eligibility criteria

18 years of age or above, [+5]

Patients under 18 years of age, [+4]

Status: Recruiting

The Effect of Hypnosis on Periodontal Treatment

Treatment of periodontal diseases relies on the mechanical removal of microbial dental plaque, calculus, and necrotic cementum from root surfaces in both supra- and subgingival areas to control inflammation in periodontal tissues. As in all dental treatments, dental phobia and dental anxiety are common challenges in initial periodontal therapy. Hypnosis is among the traditional non-pharmacological behavior management techniques used to manage stress and improve pain tolerance. It is known that hypnosis is effective in anxiety control in dentistry. The use of salivary levels of inflammatory mediators released during the disease is a valid method for assessing the progression of periodontal disease and healing after treatment. In this study, the effect of hypnosis on healing in patients undergoing Phase I periodontal therapy will be evaluated by comparing the mean differences in cytokine levels between case and control groups

Participants needed: 50
Trial details
Age: 20-65Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Feb 5, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

The Effects of Whirlpool and Contrast Bath in Patients with Complex Regional Pain Syndrome After Distal Radius Fracture

The aim of our study is to investigate the effects of whirlpool bath and contrast bath treatments on pain, disability, functionality and grip strength in patients with complex regional pain syndrome after distal radius fracture.

Participants needed: 40
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Afyonkarahisar Health Sciences UniversityUpdated: Jan 30, 2025Locations: 1
Eligibility criteria

Patients with complex regional pain syndrome type-1 (CRPS-type 1) after distal r...

Orthopedic injuries (other accompanying orthopedic fractures, such as ulna fract... [+9]