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Clinical Trials/NCT02627014
NCT02627014
Completed
Not Applicable

Effect of Treatment of Temporomandibular Joint in Patients With Chronic Migraine and Temporomandibular Disorders

Cardenal Herrera University1 site in 1 country45 target enrollmentJuly 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Migraine
Sponsor
Cardenal Herrera University
Enrollment
45
Locations
1
Primary Endpoint
Headache Impact Test (HIT-6)
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The aim of this study is to determine whether treatment of temporomandibular joint is more effective than usual care in patients with chronic migraine and temporomandibular disorders to reduce pain.

Detailed Description

The aim of this study is to determine whether treatment of temporomandibular joint added to the control group treatment and drug therapy patient base is more effective than just using the control group treatment and drug therapy in patients with chronic migraine and temporomandibular disorders to reduce pain and improve the quality of life related to health of patients.

Registry
clinicaltrials.gov
Start Date
July 2015
End Date
March 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Cardenal Herrera University
Responsible Party
Principal Investigator
Principal Investigator

Eva Segura Ortí

Eva Segura Ortí (PhD)

Cardenal Herrera University

Eligibility Criteria

Inclusion Criteria

  • Chronic migraine (ICHD_III beta, 2013)
  • Temporomandibular disorders (RDC/TMD)

Exclusion Criteria

  • other neurological disease
  • psychiatric diseases
  • Physical therapy treatment in the last 6 months
  • dental treatment in the last 6 months
  • surgery or trauma in the orofacial region

Outcomes

Primary Outcomes

Headache Impact Test (HIT-6)

Time Frame: 3 months

Secondary Outcomes

  • Quality of life (SF-36)(3 months)
  • Sleep Quality(3 months)
  • Pain catastrophizing scale (PCS)(3 months)
  • Craniofacial Pain and Disability Inventory (CF-PDI)(3 months)
  • Tampa scale of Kinesiophobia (TSK)(3 months)
  • Maximal Mouth Opening pain free(3 months)
  • Visual Analogue Scale (VAS)(3 months)
  • Pain threshold pressure(3 months)
  • Tampa scale of Kinesiophobia of cranio-mandibular disorder (TSK-TCM)(3 months)

Study Sites (1)

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