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NOT YET RECRUITING
NCT07371481
NA

CTG Versus Collagen Matrix for Peri-Implant Soft Tissue Augmentation

Sponsor: Hanoi Medical University

View on ClinicalTrials.gov

Summary

This randomized controlled trial compares two techniques for peri-implant soft tissue augmentation in the mandibular molar region: an autogenous connective tissue graft (CTG) and a collagen matrix. Adult patients requiring implant treatment with insufficient peri-implant soft tissue thickness will be randomly assigned to receive either CTG or a collagen matrix at the time of implant surgery. The study aims to evaluate and compare changes in peri-implant soft tissue thickness, width of keratinized tissue, and soft tissue contour over a 9-month follow-up period, as well as the occurrence of postoperative complications. The results of this study will help determine whether a collagen matrix can provide clinical outcomes comparable to those of connective tissue grafting for peri-implant soft tissue augmentation.

Official title: Results of Soft Tissue Grafting Around Implant in the Mandible Molar Area

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

46

Start Date

2026-02

Completion Date

2028-12

Last Updated

2026-01-29

Healthy Volunteers

No

Interventions

DEVICE

Collagen Matrix

A porcine-derived collagen matrix is used for peri-implant soft tissue augmentation at the time of implant surgery, serving as a substitute for autogenous connective tissue grafting.

PROCEDURE

Connective Tissue Graft

An autogenous connective tissue graft harvested from the patient is used for peri-implant soft tissue augmentation at the time of implant surgery.

Locations (1)

Hanoi Medical University

Hanoi, Vietnam