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Completed
NCT07698678
Evaluation of Using Patient Specific Ultra-High Molecular Weight Polyethylene Implant Versus Patient Specific Titanium Implant in Treatment of Chronic Condylar Dislocation A Randomized Control Trial
Conditions: Recurrent Dislocation of Temporomandibular Joint (Disorder)
Sex: All
Ages: 18 Years – 48 Years
Healthy volunteers: No
Phase: NA
Enrollment: 20
Sponsor: Cairo University
Location: Cairo University Cairo Cairo Governorate
Summary
Does patient specific Ultra-High Molecular Weight Polyethylene implant eminoplasty will decrease maximum interincisal distance, provide better soft tissue response and post-operative patient satisfaction than patient specific Titanium eminoplasty in treatment of chronic condylar dislocation?
Eligibility Criteria
Inclusion Criteria:
* patients with recurrent dislocation with their maximum inter incisal opening over 55mm
* longstanding dislocation of the TMJ involving both fixation for more than 3weeks and the failure of manual reduction
* failure of conservative strategies such as orientation to self-limiting jaw movement and the use of chin-cap or bandage
Exclusion Criteria:
* patients with post-menopausal females with osteoporosis
* Patient with uncontrolled systemic disease
* pregnancy
* psychological disorders, drug or alcohol dependency
* Known allergies or sensitivities to dental materials, including Zirconia, Titanium or general anesthetic agents
* Inability to return for follow up visits.
* Refusal of participation from the patient
Source: ClinicalTrials.gov (NCT07698678). StuddyBuddy aggregates publicly available trial information.