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Clinical Trials/NCT06606041
NCT06606041
Active, Not Recruiting
N/A

Comparison of the Efficacy of Dry Needling, Ischemic Compression, and Cross Taping on Masseter Myofascial Pain: A Randomized Clinical Trial

University of Coimbra2 sites in 2 countries60 target enrollmentJanuary 10, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Temporomandibular Joint Disorders
Sponsor
University of Coimbra
Enrollment
60
Locations
2
Primary Endpoint
Pain intensity
Status
Active, Not Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to learn whether Dry Needling, Ischemic Compression, and Cross Tapes work to treat myofascial pain in masseter muscles in adults. It will also learn about the safety of this treatment. The main questions it aims to answer are:

  • Do Dry Needling, Ischemic Compression, and Cross Tapes relieve masseter muscle pain?
  • Which of these treatments provides the best relief from masseter muscle pain? Researchers will compare these three treatments to see which is best for treating masseter muscle pain.

Participants will:

Treated with Dry Needling or Ischemic Compression or Cross Tapes only once Visit the clinic one week, three months, and six months after treatment.

Detailed Description

The taut band represents the most commonly observed muscular disorder, where myofascial trigger points may arise, causing referred pain in another location. Therapeutic strategies applied for its treatment include dry needling, ischemic compression, and cross-taping. Objectives: To compare the effectiveness of these treatment methods in reducing or alleviating the intensity of pain in the masseter. In this multicenter randomized clinical trial, the study sample underwent a clinical examination according to the Diagnostic Criteria for Temporomandibular Disorders to diagnose the presence of orofacial myofascial pain with taut bands in the masseter. Participants were randomly allocated to three groups based on the treatment methods.

Registry
clinicaltrials.gov
Start Date
January 10, 2024
End Date
December 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bruno Macedo de Sousa

Professor

University of Coimbra

Eligibility Criteria

Inclusion Criteria

  • Patients with myofascial pain diagnosed according Diagnostic Criteria for Temporomandibular Disorders (DC-TMD).

Exclusion Criteria

  • Pregnant women
  • Other TMD-spectrum pathologies
  • Anticoagulated and antiaggregated individuals
  • Blood disorders
  • Fibromyalgia
  • Autoimmune diseases in acute stages
  • Neurological diseases
  • Malignant tumor pathologies
  • Patients with aichthyophobia
  • Concomitant medication (opioids, antidepressants, myorelaxants)

Outcomes

Primary Outcomes

Pain intensity

Time Frame: At baseline, immediately after the intervention, 1 week, and 1 month after treatment

Pain intensity will be assessed using the Numerical Pain Rating Scale, where 0 represents the absence of pain, and 10 describes the worst possible pain.

Study Sites (2)

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