Alveolar Bone Resorption Clinical Trial
Official title:
Clinical, Radiographic and Histomorphometric Comparison of Autogenous Demineralized Dentin Matrix Versus Bovine-Derived Xenograft for Socket Preservation: A Randomised Controlled Clinical Trial
The present study is a human, prospective, randomised controlled clinical trial will be conducted to explore and compare the clinical, radiographic and histomorphometric outcome of autogenous demineralised dentin(DDM) versus bovine derived xenograft(DBM) for socket preservation procedure.
- After local anesthesia a full thickness flap will be minimally reflected buccally and
lingually around the tooth not exceeding 3mm apical to the alveolar crest.
- Tooth extraction will be performed using atraumatic extraction methods using Periotome.
- After extraction, the socket will be thoroughly curetted, inspected and irrigated with
sterile saline solution.
- The socket satisfying the inclusion and exclusion criteria will be randomly allocated to
either test or control group.
- Intra surgical measurements will be recorded.
- Socket preservation will be performed with either Demineralized dentin matrix DDM(TEST)
or bovine derived xenograft DBM (CONTROL). Bone graft will be extended to the height of
intra proximal bone.
- Collagen membrane will be placed over the grafted site extending approximately 3mm
apical to buccal and lingual crest.
- Flaps will be approximated with sutures.
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