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Clinical Trials/RBR-795k8m
RBR-795k8m
Not yet recruiting
未知

The efficacy of occlusal stabilization appliance associated to counselling in the management of myofascial pain chronic and in the improvement of the quality of life of patients with temporomandibular disorders

niversidade Federal de Juiz de Fora0 sitesMarch 31, 2012

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
niversidade Federal de Juiz de Fora
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 31, 2012
End Date
TBD
Last Updated
2 years ago
Study Type
Intervention
Sex
Female

Investigators

Sponsor
niversidade Federal de Juiz de Fora

Eligibility Criteria

Inclusion Criteria

  • All subjects participated in this study volunteers by signing the consent form. Inclusion criteria are as follows:
  • female subjects;
  • aged 20 to 55 years;
  • irrespective of race, social status or religion;
  • presence of pain intensity of at least moderate (at least 4\.0 on VAS), shown in the first clinical assessment;
  • diagnosis of myofascial pain persisting for a minimum period of six months.

Exclusion Criteria

  • history of psychiatric disorders or treatment for neurological or psychological disorders;
  • volunteers with severe intellectual or physical disability that would hinder the collection of data;
  • history of systemic diseases that generate joint symptoms, muscle or rheumatologic, such as rheumatoid arthritis and fibromyalgia;
  • pain attributed to a well\-defined local cause, such as pulpitis, trigeminal neuralgia and cancer pain;
  • attributable to migraine pain or infection;
  • report of any previous treatment for TMD;
  • treatment with drugs affecting the central nervous system (muscle relaxants, anticonvulsants, opioids, and antidepressants) and treatment with analgesics and anti\-inflammatory drugs, with or without prescription, concomitant therapies to be instituted in this research;
  • report of facial trauma as a possible etiology of TMD;
  • subject denture wearers an upper or lower;
  • volunteers aged under 20 or over 55 years;

Outcomes

Primary Outcomes

Not specified

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