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Clinical Trials/RBR-2nywjd
RBR-2nywjd
Active, not recruiting
未知

Therapeutical efficacy of two clinical protocols for Viscosuplementation of Temporomandibular joint in patients with Osteoarthritis

Faculdade de Odontologia Universidade Federal do Rio de Janeiro0 sitesStarted: September 1, 2020Last updated:

Overview

Phase
未知
Status
Active, not recruiting
Sponsor
Faculdade de Odontologia Universidade Federal do Rio de Janeiro

Overview

Brief Summary

No summary available.

Study Design

Study Type
Intervention

Eligibility Criteria

Ages
18Y to 65Y (—)

Inclusion Criteria

  • It will be included individuals of both genders, literacy, over 18 years, presenting at least one of the following symptoms: unilateral or bilateral TMJ pain, occurring spontaneously and/or during mandibular function; presenting joint noises: crepitation or click, unilateral or bilateral; mouth opening limitation and articular pain during palpation of the TMJ, either unilateral or bilateral. All study subjects must meet the criteria of group III of the Research Diagnostic Criteria for Temporomandibular Disorders (RDC\-TMD). Each individual should have a CT scan showing one or more of the following changes: joint erosion, proven by loss of normal cortical bone design; sclerosis of parts or all of the condyle and/or joint eminence; flattening of joint surfaces; presence of osteophyte; presence of subchondral cysts.

Exclusion Criteria

  • Individuals who do not meet the inclusion criteria; history of TMJ surgery; volunteers with impaired verbal communication due to neurological disorder, previous disease sequelae or psychiatric condition; pregnant women; individuals taking osteoarthritis modifying medications such as condoitine, glucosamine or diacerin; illiterate individuals

Investigators

Sponsor
Faculdade de Odontologia Universidade Federal do Rio de Janeiro

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