Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06806111

Wound Healing and Patient-Reported Outcomes After Gingival Graft Harvesting From the Palate

Led by Universitat Internacional de Catalunya · Updated on 2026-04-09

66

Participants Needed

1

Research Sites

82 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to evaluate whether two different techniques for treating palatal wounds-sutures and cyanoacrylate bioadhesive-can influence postoperative morbidity, clinical healing, and soft tissue dimensional changes in patients undergoing epithelialized gingival graft harvesting from the palate. The main questions it aims to answer are: Does the use of cyanoacrylate bioadhesive reduce postoperative morbidity compared to sutures? Does the choice of wound treatment technique affect clinical healing and three-dimensional changes in soft tissues? Researchers will compare the sutures (control group) to the cyanoacrylate bioadhesive (test group) to determine if the bioadhesive leads to improved postoperative outcomes. Participants will: Undergo epithelialized gingival graft harvesting from the palate. Receive either sutures or cyanoacrylate bioadhesive for wound closure. Be monitored for postoperative morbidity, clinical healing, and soft tissue dimensional changes.

CONDITIONS

Official Title

Wound Healing and Patient-Reported Outcomes After Gingival Graft Harvesting From the Palate

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Systemically healthy individuals older than 18 years old
  • Healthy periodontal status according to the AAP/EFP definition
  • Full-mouth plaque and bleeding scores (FMPS and FMBS) less than or equal to 20%
  • No history of soft tissue harvesting
Not Eligible

You will not qualify if you...

  • Pregnancy or lactation
  • Self-reported smoking of 10 or more cigarettes per day
  • Metabolic diseases that negatively affect soft tissue healing (e.g., diabetes mellitus)
  • Any medication that may interfere with wound healing
  • Removable maxillary prostheses
  • Ongoing orthodontic therapy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clínica Universitària d'Odontologia - UIC Barcelona

Barcelona, Sant Cugat Del Valles, Spain, 08195

Actively Recruiting

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Research Team

L

Lory Abrahamian, DDS, MSc, PhD Candidate

CONTACT

G

Gonzalo Blasi, DDS, MS, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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