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Influence of Stabilization Splint Thickness on The Temporomandibular Disorders

Temporomandibular Disorder Clinical Trial

Official title:
Influence of Stabilization Splint Thickness on The Temporomandibular Disorders

Clinical Trial Summary

The aim of the study is assessing the effect of the stabilization splint (SS) thickness on the temporomandibular disorder's and their symptoms; such as muscle or temporomandibular joint (TMJ) pain, TMJ sounds, and limitation of mouth opening.

Clinical Trial Description

Participants are selected from patients who applied to the clinic with the complaint of temporomandibular disorders (TMDs). Symptoms are evaluated with RDC/TMD forms. Regarding the treatment plan, patients are divided into two groups; 2 mm-thick splint group (2 mm-TSG) and 4 mm-thick splint group (4 mm-TSG). They used SS's at night for 8 hours, and they were recalled on 1st, 2nd, 3rd, and 6th months after splint insertion. Their symptoms and splints are checked. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04524806
Study type Interventional
Source Istanbul Medipol University Hospital
Contact
Status Completed
Phase N/A
Start date July 1, 2013
Completion date January 30, 2015
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