Vestibular Socket Therapy in Immediate Implants With Grafting Materials
- Conditions
- Dental ImplantTooth ExtractionExtarction Socket
- Interventions
- Other: VST with collagen plug soaked in bloodOther: VST with a particulate bone graft composed of two thirds autogenous cortical chips harvested from the surgical site and one third of bovine deprotinzed particlesOther: VST with Allograft Demineralized bone matrix Grafton
- Registration Number
- NCT04957654
- Lead Sponsor
- Mohamed Mofreh Hamada Hamed
- Brief Summary
The current research aims at evaluating the outcomes of the vestibular socket therapy in immediate implants using collagen plug, demineralized freeze-dried bone allograft, and deproteinized bovine bone minerals at both radiographic and clinical levels
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 24
- Patients will be included if they have one or more hopeless teeth without signs of acute infection in the maxillary anterior region.
- Remaining roots or non-restorable teeth with sufficient bone apically and palatably to allow proper implant positioning with sufficient primary stability.
- Optimal compliance as evidenced by no missed treatment appointments and a positive attitude towards oral hygiene.
- Medically free
- Medically compromised patients and systemic conditions precluding implant and periodontal surgery.
- Smokers, diabetics, pregnant or lactating women.
- History of chemotherapy, radiotherapy in head and/or neck region.
- Bisphosphonate therapy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description VST with collagen plug soaked in blood VST with collagen plug soaked in blood - VST with autogenous cortical chips and bovine deprotinzed particles VST with a particulate bone graft composed of two thirds autogenous cortical chips harvested from the surgical site and one third of bovine deprotinzed particles - VST with Allograft Demineralized bone matrix Grafton VST with Allograft Demineralized bone matrix Grafton -
- Primary Outcome Measures
Name Time Method changes in facial plate height at baseline, 6 and 12 months Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess height of labial (facial) plate of bone and implant survival
changes in facial plate thickness at baseline, 6 and 12 months Each group will be subjected to: Cone beam computed tomography (CBCT) at baseline, 6 months, and 12months to assess the thickness of the labial (facial) plate of bone and implant survival
- Secondary Outcome Measures
Name Time Method changes in peri-implant mucosal level at baseline, 3rd and 6th months Each group will be subjected to Intraoral scanning at baseline, 6 months and 12 months. The changes in peri-implant mucosal level will be assessed by superimposition of scanning files of different intervals to monitor the changes in surface area calculated by software.
Trial Locations
- Locations (1)
Faculty of Dentistry, Tanta University
🇪🇬Tanta, Egypt