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Gingival Recession clinical trials

View clinical trials related to Gingival Recession.

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NCT ID: NCT03954028 Withdrawn - Clinical trials for Gingival Recession, Generalized

The Healing of Soft Tissue Augmentation by Acellular Dermal Matrix and Autogenous Subepithelial Connective Tissue Graft

Start date: March 2021
Phase: N/A
Study type: Interventional

The study team proposes to prospectively compare the healing outcomes of autogenous soft tissue connective tissue graft (CTG) and Acellular dermis matrix (ADM) in a split-mouth design study for patients requiring modification of gingival soft tissue biotype. The researchers aim to investigate the earlier phase of graft healing after the grafting surgery by biopsy histology and by examining the alteration of gene profile during the healing of gingival tissue healing by molecular cell biological techniques.

NCT ID: NCT03734458 Withdrawn - Gingival Recession Clinical Trials

Platelet Rich Fibrin and Autologous Fibrin Glue

Start date: July 2019
Phase: N/A
Study type: Interventional

Platelet-rich fibrin (PRF) and Autologous Fibrin Glue (AFG) are fibrin preparation derived from human blood samples and are used in regenerative dentistry. Aim: The aim of this study is to evaluate the level of root coverage using PRF (+) AFG with a coronally advanced flap (CAF) or PRF only with a CAF compared to a sub-epithelial connective tissue graft (CTG) with a CAF for treating Class 1 and 2 gingival recession defects. Additionally, to evaluate the level of keratinized tissue tissue thickness and width using PRF (+) AFG with a CAF or PRF only with a CAF compared to CTG with CAF for Class 1 and 2 gingival recession defects. Method: 48 patients with recession defects will be randomly divided into three different treatment groups. Treatment Group A (n=16) will consist of patients treated with PRF (+) AFG with a CAF, Group B (n=16) will consist of patients treated with PRF only with a CAF and Group C (n=16) will consits of patients treated with CTG with CAF as a control. Clinical measurements will be assessed at baseline and at 1 month and 6 months after the surgery. The clinical measurements that will be recorded, include probing depth, clinical attachment level, and gingval recession parameters. The gingival recession parameters include recession width, depth and thickness.

NCT ID: NCT02810067 Withdrawn - Gingival Recession Clinical Trials

Root Coverage Comparing an Allograft to a Bovine Xenograft

Start date: June 2016
Phase: N/A
Study type: Interventional

Root coverage with acellular dermal matrix using the coronally positioned tunnel technique comparing two different donor materials