clinical random trial to evaluate the effectiveness and volume of fat that placed inside the joint which available near to jaw joint and fat from abdomen, is done for the treatment of fused jaw joint.
Phase 3
Completed
- Conditions
- Health Condition 1: null- TMJ ankylosis
- Registration Number
- CTRI/2016/04/006839
- Lead Sponsor
- all india institute of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
•All patient with unilateral/bilateral TMJ ankylosis.
•Age > 5 years and below 50 years.
•Patients giving consent for the study
Exclusion Criteria
•Metabolic fat disorders.
•Local pathology in lower abdomen and buccal mucosal areas.
•Patients refusing consent for follow up or investigations.
•Pregnant patient.
•Patients with any other underlying systemic disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method abdominal fat will remain in tmj after 1 year with less shrinkage in volume <br/ ><br>mouth oppening will be more in abdominal fat groups <br/ ><br>upper air way volume will evaluatedTimepoint: abdominal fat will remain in tmj after 1 year with less shrinkage in volume <br/ ><br>mouth oppening will be more in abdominal fat groups <br/ ><br>upper air way volume will evaluated
- Secondary Outcome Measures
Name Time Method 1.To evaluate the maximum incisal opening between two groups. <br/ ><br>2.To evaluate the upper airway volume within one month and 1 year after interpositional temporomandibular joint arthoplasty. <br/ ><br>3.To evaluate the functional efficacy of pedicled buccal pad of fat and abdominal fat in temporomandibular joint arthoplasty <br/ ><br>Timepoint: one year after surgery