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Clinical Trials/CTRI/2024/02/063310
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

Sponsor
il

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