Comparison of Autogenous Bone Graft and Screw Tent-Pole Technique on Atrophic Mandible
Alveolar Bone Loss
About this trial
This is an interventional treatment trial for Alveolar Bone Loss focused on measuring Bone augmentation, Autogenous block bone graft, Leukocytes and platelet-rich fibrin, Injectable platelet rich fibrin, Tent-pole technique
Eligibility Criteria
Inclusion Criteria:
- Patients who refused to use a partially removable prosthesis and requested dental implant treatment,
- Patients had bilateral, moderate or severe posterior atrophic mandible,
- Patients had precluded conditions suitable for short dental implant.
Exclusion Criteria:
- Patients who had systemic diseases (osteoporosis, hemophilia, anemia, etc.),
- Patients who required drugs (bisphosphonate or steroid therapy),
- Patients who had a smoking habit,
- Patients who had received radiation therapy within the last two years,
- Patients who were under 18 years old, pregnant or lactating,
- Patients who had a total platelet count lower than 150,000/mm3.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Autogenous block bone graft
i-PRF enriched allograft material+screw tent pole technique
Surgical site as control group was treated with autogenous block bone graft. Augmentation site was covered with a mixture of particulate allograft and leukocyte and platelet-rich fibrin (L-PRF) membrane.
Surgical site as test group was treated with injectable platelet rich-fibrin (i-PRF) enriched allograft material. To avoid soft tissue collapse, screws were used. Augmentation site was covered with leukocyte and platelet-rich fibrin (L-PRF) membrane.