Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07409558

Three-Dimensional Digital Evaluation of Soft Tissue Changes After Modified and Conventional Free Gingival Graft Surgery: A Randomized Controlled Trial

Led by Kahramanmaras Sutcu Imam University · Updated on 2026-02-13

34

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of two types of free gingival graft surgeries—conventional free gingival graft (FGG) and modified free gingival graft (ModFGG)—on soft tissue thickness, volume, and creeping attachment in the lower front teeth. This trial involves 34 healthy, non-smoking adults with localized Cairo Class II gingival recession. The goal is to understand how the modified technique may improve soft tissue stability and volume compared to the conventional method, using advanced three-dimensional digital analysis. Participants will be randomly assigned to receive either the conventional FGG procedure or the modified ModFGG procedure. The ModFGG involves creating a connective tissue flap from the recession area to cover the exposed root before placing a graft from the palate, aiming to enhance blood supply and healing. The conventional FGG involves placing a graft from the palate directly onto the prepared site without this flap. Both procedures will be followed by digital and clinical assessments at baseline, and at 1, 3, and 6 months after surgery. During the study, participants will undergo clinical measurements including gingival recession depth, keratinized tissue width, and probing depth, alongside three-dimensional digital scans with an intraoral scanner to evaluate soft tissue thickness and volume changes. These evaluations at multiple time points will help assess tissue stability and healing progress. The study will last at least six months post-surgery, providing detailed information on soft tissue outcomes and healing after these grafting procedures.

CONDITIONS

Brief Title

3D Digital Assessment of Soft Tissue Changes After Modified FGG

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Systemically healthy individuals
  • Non-smokers
  • Localized Cairo Class II gingival recession with vertical depth of at least 3 mm on the lower front teeth
  • Probing pocket depth of 3 mm or less at the treated tooth/teeth
  • No tooth mobility (grade 1 or less)
  • No cervical composite restorations or non-carious cervical lesions
  • Presence of a shallow vestibule (less than 5 mm)
Not Eligible

You will not qualify if you...

  • Pregnancy or breastfeeding
  • Untreated periodontal disease
  • Presence of parafunctional habits
  • Poor oral hygiene with plaque score over 20%
  • Malpositioned, rotated, or crowded teeth in the front gum area
  • Known systemic diseases such as AIDS or diabetes
  • Conditions or medications affecting gum healing
  • ASA physical status classification III or higher

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single treatment visit with follow-up assessments up to 6 months

Participants will undergo either a modified free gingival graft (ModFGG) or a conventional free gingival graft (FGG) procedure to treat gingival recession and improve soft tissue stability.

1 treatment visit and 3 follow-up visits at 1, 3, and 6 months postoperatively

Trial Site Locations

Total: 1 location

1

Kahramanmaraş Sütçü İmam University

Kahramanmaraş, Kahramanmaraş, Turkey (Türkiye), 46000

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Research Team

E

esra bozkurt

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

Modified free gingival graft technique for treatment of gingival recession defects at mandibular incisors: A randomized clinical trial.

Olivier Carcuac, Anna Trullenque-Eriksson, Jan Derks

https://pubmed.ncbi.nlm.nih.gov/36627509