Efficacy of BoNT-A treatment in patients with Awake Bruxism and Temporomandibular Disorder (TMD)
Phase 2
- Conditions
- BruxismC05.500.607.221.897.897
- Registration Number
- RBR-62cftbp
- Lead Sponsor
- Faculdade de Odontologia da Universidade do Estado do Rio de Janeiro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Volunteers of both genders; aged between 18 and 60 years; with Temporomandiibular Disorders; With high frequency of awake bruxism activity
Exclusion Criteria
Volunteers with facial and Temporomanbular Joint trauma; using full dentures or removable partial dentures; ongoing orthodontic treatment; blood dyscrasia patients; with presence of arthritis; arthrosis; diabetes; neurological pathologies; fibromyalgia; who received tetanus vaccine or botulinum toxin injections in the three months prior to the study
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method