Horizontal Ridge Augmentation of the Mandible Autogenous Block Grafts
- Conditions
- Horizontal Ridge DeficiencyBlock Graft
- Interventions
- Procedure: ridge split interpositional block graftProcedure: decortication Onlay block graft
- Registration Number
- NCT03183336
- Lead Sponsor
- Cairo University
- Brief Summary
20 subjects presenting with horizontal mandibular ridge width less than 5 mm were selected and randomly divided two groups (10 in each group). the first group received interpositional block grafts (harvested from the chin and ramus) covered with Platelet-rich fibrin membrane. the second group received onlay block grafts (harvested from the chin and ramus) and covered with Platelet-rich fibrin membrane. the grafts are left for 4 months. the alveolar ridge width dimensions is then measured using radiographic analysis using cone-beam computed tomography scans
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
- Patients of both sexes with a minimum vertical bone height above the inferior alveolar canal of 10mm in the edentulous region.
Patients should have ridge thickness less than 5mm measured 2mm from the alveolar crest Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.
- Patients with any systemic disease that may affect normal bone healing. Patients with drug allergies, drug or alcohol abuse, periodontal diseases or poor oral hygiene
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Interpositional block graft ridge split interpositional block graft ridge split interpositional block graft Onlay block graft decortication Onlay block graft decortication onlay block graft
- Primary Outcome Measures
Name Time Method alveolar ridge width gained 4 months radiographic analysis following ridge augmentation using Cone beam computed tomography
- Secondary Outcome Measures
Name Time Method patient morbidity following the surgical procedure 14 days pain value on pain scale