Masseter Muscle

5

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

Condition / disease
Location
Status: Not yet recruiting

Postoperative Bite Force After Bioflx and Zirconia Crowns in Children

This randomized clinical trial aims to compare postoperative bite force following full-crown restoration with preformed Bioflx and zirconia crowns in children undergoing comprehensive dental treatment under general anesthesia. Children aged 4-7 years requiring full-coverage restoration of primary molars will be randomly allocated to receive either Bioflx or zirconia crowns. Occlusal bite force will be assessed before treatment and at predefined postoperative follow-up time points using a digital occlusal analysis system. The study will evaluate changes in occlusal function following placement of the two types of pediatric full-coverage crowns.

Participants needed: 30
Trial details
Age: 4-7Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Sep 18, 2026Locations: 1
Eligibility criteria

Children aged 4-7 years. [+5]

Children with systemic diseases or medical conditions that may affect oral healt... [+4]

Status: Not yet recruiting

Bite Force Recovery Following Pediatric Full Crown Restorations

A component of masticatory function is bite force. Dental caries is one factor that contributes to poor dental health, which has an overall negative influence on quality of life. Caries has a detrimental after effect of functional impairment. this study aims to evaluate how children occlusal bite forces are affected by complete dental care. thirty children with dental caries in their primary molars, ages 5 to 8, of both sexes will be included. Occlusal force gauge was used to measure the occlusal bite force in the vicinity of primary molars both before and after restorations. A statistical analysis was performed on the collected data

Participants needed: 30
Trial details
Age: 5-8Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Aug 31, 2026Locations: 1
Eligibility criteria

Children aged 5-8 years. [+8]

Temporomandibular joint disorders [+4]

Status: Not yet recruiting

Efficacy of PRP Injections in Reducing Pain for Myogenous TMD Patients

This study aims to evaluate whether intramuscular injections of platelet-rich plasma (PRP) are more effective than isotonic saline in reducing pain and improving jaw function in individuals diagnosed with myogenous temporomandibular disorders (TMD). Myogenous TMD is a common source of orofacial muscle pain and functional limitation, and although conservative treatments help many patients, a significant proportion continue to experience persistent symptoms that affect daily life and quality of function. PRP is an autologous, minimally invasive biologic concentrate enriched with platelets and bioactive molecules that may promote tissue repair and modulate inflammation, making it a promising option for managing muscle-related pain conditions. However, evidence from well-controlled randomized clinical trials in myogenous TMD remains limited. In this double-blind, randomized controlled clinical trial, participants will receive two intramuscular injections-either PRP or saline-administered one month apart. Follow-up assessments will occur at 1, 3, and 6 months using standardized and validated measures of pain intensity, pain sensitivity, mandibular function, and psychosocial factors. The results of this study may help determine the clinical value of PRP for myogenous TMD and contribute to future standardization of regenerative treatment protocols in orofacial pain management.

Participants needed: 50
Trial details
Age: 20-50Biological sex: FemaleType: InterventionalSponsor: Karolinska InstitutetUpdated: Aug 5, 2026Locations: 1
Eligibility criteria

women 20 to 50 years with a confirmed diagnosis of myogenous TMD according to th... [+3]

active infection or inflammation at the injection site [+13]

Status: Not yet recruiting

Masseter Muscle Thickness in Individuals With Chronic Neck Pain

The primary objective of our study is to compare the thickness of the masseter muscle, measured by ultrasound, in individuals with chronic neck pain to that of healthy individuals. The secondary objective of the study is to examine the relationships between masseter muscle thickness and pain intensity, neck disability level, pain catastrophizing level, and clinical diagnostic criteria in individuals with chronic neck pain.

Participants needed: 90
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Hasan Kalyoncu UniversityUpdated: Mar 13, 2026Locations: 1
Eligibility criteria

Be between the ages of 18 and 45 [+2]

History of cervical spine surgery or severe trauma [+7]

Status: Recruiting

Evaluation of the Effect of Adenoid Hypertrophy on the Masseter Muscle in Children: A Comparative Ultrasonographic Study

The goal of this observational study is to evaluate the effect of adenoid hypertrophy on the masseter muscle in children aged 3 to 8 years. The primary objectives are: * To assess whether adenoid hypertrophy affects the thickness or structure of the masseter muscle. * To determine whether there is a measurable difference in masseter muscle characteristics between children with and without adenoid hypertrophy. Researchers will compare children diagnosed with adenoid hypertrophy and scheduled for adenoidectomy to healthy controls without adenoid hypertrophy. Each participant will: * Undergo ultrasonographic examination of the masseter muscle using a 9L linear probe (6-15 MHz), and * Have their occlusal relationship, dental findings, age, sex, and adenoid hypertrophy grade recorded.

Participants needed: 72
Trial details
Age: 3-8Biological sex: AllType: ObservationalSponsor: Melis AKYILDIZUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

Children aged between 3 and 8 years [+2]

Children with a history of surgery for adenoid hypertrophy [+3]