Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05729607

Vertical Soft Tissue Augmentation With CTG vs ADM

Vertical Soft Tissue Augmentation With Dermal Matrix and Enamel Matrix Derivative vs Connective Tissue Graft for the Treatment of Peri-implant Soft Tissue Dehiscences in the Esthetic Zone: A Randomized, Controlled, Clinical, Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
28 (estimated)
Sponsor
Harvard Medical School (HMS and HSDM) · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Accepted

Summary

The study aims at comparing two different approaches for vertical soft tissue augmentation at implant sites exhibiting soft tissue dehiscences: autogenous connective tissue graft vs acellular dermal matrix + enamel matrix derivative

Detailed description

The present randomized clinical trial aims at investigating two approaches (autogenous connective tissue graft vs acellular dermal matrix + enamel matrix derivative) when performed for vertical soft tissue augmentation at sites with peri-implant soft tissue dehiscences. Clinical, volumetric, ultrasonographic, and patient-reported outcomes will be evaluated at different time points up to 1 year.

Conditions

Interventions

TypeNameDescription
PROCEDUREVertical soft tissue augmentationVertical soft tissue augmentation with autogenous connective tissue graft (CTG)
PROCEDUREVertical soft tissue augmentationVertical soft tissue augmentation with acellular dermal matrix (ADM) and enamel matrix derivative (EMD)

Timeline

Start date
2023-05-26
Primary completion
2027-02-27
Completion
2027-11-27
First posted
2023-02-15
Last updated
2025-09-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05729607. Inclusion in this directory is not an endorsement.