Randomised clinical trial in subjects with temporomandibular dysfunction treated with Michigan Splint versus CAD/CAM Splint

Not Applicable

• Conditions: K07.6; F45.8; Temporomandibular joint disorders; Other somatoform disorders

• Registration Number: DRKS00004275
• Lead Sponsor: Poliklinik für Zahnärztliche Prothetik der Ludwig-Maximilians-Universtät München

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-08-09
• Study Completion: 2013-10-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 35

Inclusion Criteria

Temporomandibular dysfunction

Exclusion Criteria

-Subjects younger than 20 years and older than 60 years-old.
-Subjects having at the moment another disease that is not the TMD and that causes pain ( for instance, sinusitis or rheumatism).
-Subjects with Orthodontics or Functional Maxillary Orthopedics or splint usage.
-Subjects with craniofacial trauma in the last 6 months.
-Subjects with muscle relaxant usage.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary outcome is the pain reduction measurement by numerical scale.<br>The measurement is going to be made befor the intervention and than monthly during 9 months.

Secondary Outcome Measures

Name	Time	Method
The secundary outcome is the change in mandibular movement that is going to be eletronically measured.<br>The measurement is going to be made before the intervention and than in 3 and 6 months.