Evaluation of the efficacy of personalized TMJ prosthesis compared to non-personalized TMJ prosthesis: a follow-up study
- Conditions
- Temporomandibular joint disordersICD K07.6
- Registration Number
- RBR-6rkgsg8
- Lead Sponsor
- Complexo de Saúde São João de Deus
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Patients 18 years or older presenting consolidated bone conformation; in advanced stages of temporomandibular joint disorders; in which traditional and conservative approaches have already been tried and have failed; such as osteoarthritis; tumors; trauma; inflammatory or degenerative pathologies of the temporomandibular joint (TMJ); autoimmune tissue connective diseases affecting the TMJ; fibrous or bone ankylosis; missing or deformed structures and spondyloarthropathies.
Patients in constant use of analgesics or anti-inflammatory drugs; syndromic; immunosuppressed; diabetic patients with uncontrolled coagulopathies; and hypertensive patients. Participants will also be excluded from the study if they have other treatment alternatives; have uncontrollable masticatory muscle hyperfunction such as bruxism; or known allergy to prothesis' material; Participants previously implanted with ATM prostheses will also be excluded from the study; as well as participants who need reconstruction that is not restricted to the branch and that encompasses the mandibular body.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method