Comparison of non-surgical treatments for temporomandibular joint disorders
Not Applicable
- Conditions
- Health Condition 1: M266- Temporomandibular joint disorders
- Registration Number
- CTRI/2024/01/061717
- Lead Sponsor
- Saumya Shukla
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients clinically diagnosed with TMD as per the latest version of DC/TMD.
Patients who have given informed consent for the study.
Patients with CBC, RA Factor and Uric Acid levels within normal limits.
Exclusion Criteria
Subjects with history of orthodontic/prosthodontic treatment.
Subjects with history of trauma/surgery of the TMJ.
Subjects with history of previous treatment for the same complaint.
Subjects who are known cases of epilepsy.
Subjects with pacemaker.
Pregnant females.
Subjects with CBCT scans showing degenerative changes in the mandibular condyle e.g. Rheumatoid Arthritis, Osteoarthritis etc.
Patients not willing to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain (NRS), maximum mouth openingTimepoint: Baseline, 1 month, 2 months, 3 months
- Secondary Outcome Measures
Name Time Method Clicking, Deviation, Joint Space (CBCT changes)Timepoint: Baseline, 1 month, 2 months, 3 months