CTRI/2024/02/063310Not yet recruitingUnknown
Comparative effectiveness of Soft Splint, Centric Stabilization Splint, andHydrostatic Splint in patients exhibiting Temporomandibular disorders- ARandomized control trial - NI
il0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Unknown
- Status
- Not yet recruiting
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Patient’s age ranging from 18 years to 45 years (both included) were included in our study.
- •2. Patients were recruited irrespective of sex, religion, caste or socioeconomic status.
- •3. RDC/TMD classification among Axis 1 were selected.
- •4. Fully dentate or at least had sufficient occlusal stops, no more than two posterior teeth missing in each quadrant (excluding third molars) were selected.
Exclusion Criteria
- •1. Completely edentulous patients or patients with no posterior occlusal stops were excluded from the study.
- •2. Patents having reduced mouth opening were excluded from the study.
- •3. Patients who had undergone previous treatment with occlusal appliances were also excluded from the study.
- •4. Patients undergoing Orthodontic treatment were excluded from the study.
- •5. Patients with pain because of systemic disease (eg; rheumatoid arthritis, etc) were also excluded from the study.
Investigators
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