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Clinical Trial Summary

The aim of the current study is to compare the effect socket sealing with flowable resin composite compared to dense polytetrafluoroethylene membrane after filling the extraction site with xenograft particles in terms of soft and hard tissue changes, procedural time, post operative pain, patients' satisfaction, and cost effectiveness.


Clinical Trial Description

Implant placement has become the gold standard for replacing missing teeth. One of the biggest challenges present when placing implants is the lack of sufficient bone dimensions. This deficiency may be a common finding due to the process of post extraction remodeling where both bone height and width are reduced, complicating implant placement. As a result, several procedures have been suggested to address this issue. Socket preservation is one of the most implemented procedures used today to limit the amount of bone lost during post extraction remodeling. The current study was designed to compare the effectiveness of using flowable composite resin for socket sealing as an alternative to using d-PTFE membranes, bypassing the added time, cost and trauma needed for tunnel preparation and membrane tucking. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06315413
Study type Interventional
Source Cairo University
Contact Youssef Meshreky, Master degree
Phone +201006382121
Email youssefmeshreky@gmail.com
Status Not yet recruiting
Phase N/A
Start date April 1, 2024
Completion date December 1, 2025

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