Clinical Trials Directory

Trials / Completed

CompletedNCT04524806

Influence of Stabilization Splint Thickness on The Temporomandibular Disorders

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
104 (actual)
Sponsor
Istanbul Medipol University Hospital · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERstabilization splintStabilization splint is an appliance which applied to upper or lower jaw and regulating the occlusal forces in the temporomandibular joint that can cause disorders, also preventing excessive contraction of the masticatory muscles

Timeline

Start date
2013-07-01
Primary completion
2014-01-01
Completion
2015-01-30
First posted
2020-08-24
Last updated
2020-08-24

Source: ClinicalTrials.gov record NCT04524806. Inclusion in this directory is not an endorsement.