Skip to main content
Clinical Trials/NCT00154128
NCT00154128
Completed
Phase 1

The Influence of of a Stabilization Splint on the Body Posture in TMD Cases and Controls

University Medicine Greifswald0 sites40 target enrollmentApril 2005

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Temporomandibular Disorders
Sponsor
University Medicine Greifswald
Enrollment
40
Primary Endpoint
changes in body posture
Status
Completed
Last Updated
20 years ago

Overview

Brief Summary

The study was designed to investigate a possible influence of an occlusal stabilization splint on the body posture in TMD cases and controls. Interocclusal appliances or occlusal splints are therapeutic devices that are most frequently used in the treatment of TMD. Changes of the mandibular position and occlusal equilibrations are assumed to have an impact on the general body posture.

Detailed Description

Thirty TMD cases and 10 controls were included in the study. All participants were recruited from the School of Dentistry, University of Greifswald. All subjects gave their written consent to participate in the study. They then completed a TMD history questionnaire and underwent a clinical examination. The examination included palpation of the masticatory muscles and the TMJs, range of mandibular motion measurements, and assessment of joint noises. The TMD cases were required to have a diagnoses of myofascial pain and/or arthralgia. Controls had to be free of pain symptoms in their masticatory muscles and TMJs. Body posture was measured during five minutes of walking using an ultrasound-distance measuring device (sonoSens® Monitor) with small sensors placed on the skin that continually record changes in the distance between them. A static posture evaluation was performed with a contactless, and radiation-free static measurement of the back surface and spine using a 3D measurement system (formetric II). A second measurement was performed after insertion of the occlusal appliance and a third one after 7 days of treatment. The occlusal appliances were inserted after the first examination and all participants were instructed to use it at night and during examinations.

Registry
clinicaltrials.gov
Start Date
April 2005
End Date
August 2005
Last Updated
20 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Medicine Greifswald

Eligibility Criteria

Inclusion Criteria

  • TMD cases: diagnoses of myofascial pain and/or arthralgia

Exclusion Criteria

  • TMD cases: chronic systemic diseases, cardiac pacemakers

Outcomes

Primary Outcomes

changes in body posture

Secondary Outcomes

  • score of compliants
  • number of tender muscles and TMJs

Similar Trials