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Vestibular Socket Therapy Using Acellular Dermal Matrix Versus Connective Tissue Graft

Immediate Implant Clinical Trial

Official title:
Vestibular Socket Therapy Using Acellular Dermal Matrix Versus Connective Tissue Graft in Immediate Implants of Aesthetic Zone

Clinical Trial Summary

The aim of this study is to evaluate and compare the Vestibular Socket Therapy (VST) technique using alloderm versus connective tissue graft both with xenogenic bone membrane in immediate implants of anterior aesthetic zone.

Clinical Trial Description

Twenty surgical sites will be divided into two groups; each of which has 10 surgical sites. Grouping will be done randomly sequentially numbered, opaque, sealed envelopes (SNOSE) The groups will be treated as follow: - Group I: Ten sites will be treated by immediate implant and VST with Alloderm + allogenic bone membrane and xenograft. - Group II: Ten sites will be treated by immediate implant and VST with connective tissue graft + allogenic bone membrane and xenograft 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. The changes in gingival phenotype could be assessed at 6 months and 12 months intervals by superimposition of DICOM files on CBCT software Each group will be subjected to Cone Beam Computed Tomography (CBCT) at baseline, 6 months and 12months to asses both thickness and height of labial (facial) plate of bone and implant survival. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06241196
Study type Interventional
Source Tanta University
Contact
Status Active, not recruiting
Phase Phase 2
Start date July 1, 2022
Completion date April 1, 2024
View Details
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