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Comparison of Autogenous Dentin Matrix Versus Bovine-Derived Xenograft for Socket Preservation

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

Clinical Trial Summary

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.

Clinical Trial Description

- 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04239378
Study type Interventional
Source Krishnadevaraya College of Dental Sciences & Hospital
Contact Dr.JOANN PAULINE GEORGE, MDS
Phone 9448541637
Email drjoannpaulinegeorge@gmail.com
Status Recruiting
Phase N/A
Start date December 10, 2019
Completion date November 2021
View Details
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