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Clinical Trials/NCT01187316
NCT01187316
Completed
Not Applicable

Massage and Transcutaneous Electrical Nerve Stimulation Therapies for Temporomandibular Disorders in Adolescents

University of Pernambuco1 site in 1 country8 target enrollmentApril 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Temporomandibular Joint Disorders
Sponsor
University of Pernambuco
Enrollment
8
Locations
1
Primary Endpoint
Pain
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

The aim of the present study was to carry out a pilot project comparing the effectiveness of two therapeutic approaches to temporomandibular disorders (TMDs) in adolescents. Eight female individuals diagnosed based on the Research Diagnosis Criteria for TMDs (RDC/TMD-axis 1)were randomly divided into two groups: 1) Massage therapy and muscle stretching (n=4); and 2) transcutaneous electrical nerve stimulation (TENS) (n=4). Regardless the treatment, ten sessions were held for each patient and two measurements (baseline and 10th session) were performed for the assessment of symptom evolution using a visual analog scale (VAS), maximum opening of the mouth (MOM) and pressure pain threshold (PPT). Statistical analysis wiil be carefully selected.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
September 2007
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
University of Pernambuco

Eligibility Criteria

Inclusion Criteria

  • Pain in orofacial area for at least 3 months
  • Diagnosed at group 1 of RDC/TMD (myofascial pain with or without mouth opening limit)

Exclusion Criteria

  • Drug use for treatment of pain
  • Functional limitations that would harm diagnosis

Outcomes

Primary Outcomes

Pain

Time Frame: Two times a week

The subjects was asked to mark the intensity of the pain on a 100mm line, which was numbered from 0 to 10, being "0" = no pain, and 10 = to the worst pain ever felt. The outcome of pain intensity was given as a number marked by the patient.

Secondary Outcomes

  • Maximum mouth opening amplitude(Two times a week)

Study Sites (1)

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