Working... Menu

Physical Therapy for Temporomandibular Joint (TMJ) Closed Lock

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01475630
Recruitment Status : Completed
First Posted : November 21, 2011
Last Update Posted : November 22, 2011
Information provided by (Responsible Party):
prof.dr. Antoon De Laat, KU Leuven

Brief Summary:
The aim of the present study was to investigate the effect of Physical Therapy (PT) on pain and mandibular function in patients with anterior disc displacement without reduction (ADD-R) or "closed lock" of the TMJ and this in a randomized controlled trial design.

Condition or disease Intervention/treatment Phase
Temporomandibular Joint Disorders Temporomandibular Joint Disc Displacement, Without Reduction Procedure: physical therapy Procedure: control Not Applicable

Detailed Description:
The study evaluated the effect of extra, technical PT over the traditional information on the benign nature of the disease and the advice to refrain from overuse or misuse of the masticatory system as in parafunctions.

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 49 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Randomised Controlled Trial on Physical Therapy PT) for TMJ Closed Lock
Study Start Date : June 2003
Actual Primary Completion Date : June 2011
Actual Study Completion Date : November 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Health Checkup

Arm Intervention/treatment
information, avoiding parafunctions
Procedure: control
Other Names:
  • counseling
  • information

Experimental: physical therapy
mobilisation, exercises ,..
Procedure: physical therapy
mobilisation of the jaw, exercises, boostering information on avoiding parafunctions
Other Name: physiotherapy

Primary Outcome Measures :
  1. pain intensity [ Time Frame: 1 year ]
    using VAS scales

Secondary Outcome Measures :
  1. mouth opening [ Time Frame: 1 year ]
    interincisal dstance measured by a ruler upon active and passive mouth opening

  2. pressure pain threshold [ Time Frame: 1 year ]
    the pressure pain threshold was measured using an algometer at the masseter and temporalis muscles bilaterally

  3. mandibular function impairment questionnaire [ Time Frame: 1 year ]
    Using a validated questionnaire the impact of the pain and limitaiton on normal masticatory function is monitored

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Layout table for eligibility information
Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • All patients were recruited from the Oral Pain and Dysfunction Clinic and strictly satisfied the RDC-TMD criteria for .for disc displacement without reduction with (group IIb) or without (group IIc) limitation of mouth opening, based upon history and clinical examination. Additionally, pain experienced during the first examination had to be ≥ 35mm on a visual analog scale (VAS) of 100mm.

Exclusion Criteria:

  • Patients were excluded if their medical history mentioned orofacial traumata (contusion or fracture), systemic disorders (e.g. rheumatoid arthritis, fibromyalgia), cervical disorders (operationalized as complaints, pain or referral patterns of pain provoked during movements of the cervical spine), neurologic disorders (e.g. trigeminal neuralgia, migraine or tension type headache), drug or alcohol abuse, use of antidepressant or hormonal medication. Participants did not receive therapy for symptoms of TMD within the last 2 months.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01475630

Layout table for location information
univ hospital sint Rafael, KULeuven
Leuven, Belgium, B-3000
Sponsors and Collaborators
KU Leuven
Layout table for investigator information
Principal Investigator: Antoon De Laat, DDS,PhD Catholic University Leuven

Publications automatically indexed to this study by Identifier (NCT Number):
Layout table for additonal information
Responsible Party: prof.dr. Antoon De Laat, Head of Service Dentistry, KU Leuven Identifier: NCT01475630     History of Changes
Other Study ID Numbers: ML2210
First Posted: November 21, 2011    Key Record Dates
Last Update Posted: November 22, 2011
Last Verified: November 2011

Keywords provided by prof.dr. Antoon De Laat, KU Leuven:
temporomandibular joint
rehabilitation medicine
joint diseases
physical therapy

Additional relevant MeSH terms:
Layout table for MeSH terms
Joint Diseases
Temporomandibular Joint Disorders
Temporomandibular Joint Dysfunction Syndrome
Musculoskeletal Diseases
Craniomandibular Disorders
Mandibular Diseases
Jaw Diseases
Muscular Diseases
Stomatognathic Diseases
Myofascial Pain Syndromes