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NCT07863882
Keratinized Tissue Augmentation Using Augmented Gingival Matrix Compared to Free Gingival Graft Around Implants
Conditions: Keratinized Tissue Augmentation Around Dental Implants
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 50
Sponsor: The Forsyth Institute
Location: ADA Forsyth Institute Somerville Massachusetts
Summary
This is a 12-month, randomized, examiner-blinded, controlled, two-arm, parallel-group, single-site clinical trial comparing a biocompatible tissue graft (Augmented Gingival Matrix barrier) with a free gingival graft (FGG) to increase the keratinized tissue around implants in medically healthy subjects. Subjects will be enrolled in a balanced manner (1:1; treatment:control) into one of the 2 following treatment arms for keratinized tissue augmentation:
1. Group A: Augmented Gingival Matrix barrier (Test group)
2. Group B: Free gingival graft (Control Group)
Eligibility Criteria
Inclusion Criteria:
* • Willing and able to abide by the terms of the consent form and sign the Informed Consent form
* Good general health as evidenced by medical history
* Ages 18 and over
* Edentulous or partially edentulous patients who had undergone dental implant surgery
* Patients exhibiting KT/mucosa width of \>0.5 but \
Source: ClinicalTrials.gov (NCT07863882). StuddyBuddy aggregates publicly available trial information.