Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07409558

3D Digital Assessment of Soft Tissue Changes After Modified FGG

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

34

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this randomized controlled clinical trial is to evaluate the effects of conventional free gingival graft (FGG) and modified free gingival graft (ModFGG) techniques on soft tissue thickness, volumetric change, and creeping attachment in mandibular incisors using three-dimensional direct digital analysis. The study will include a total of 34 systemically healthy, non-smoking individuals with localized Cairo Class II gingival recession. Participants will be randomly assigned to the FGG (control) and ModFGG (test) groups. Clinical measurements will be performed before surgery and at 1, 3, and 6 months post-surgery. Soft tissue thickness and volumetric changes will be analyzed three-dimensionally by overlaying digital models obtained with an intraoral scanner. Gingival recession depth, keratinized tissue height, and creeping attachment will also be assessed. The aim is to provide clinical evidence regarding the effects of the modified free gingival graft technique on soft tissue stability and volumetric gains.

CONDITIONS

Official 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 recession depth of �93 mm on buccal surfaces of mandibular incisors
  • Probing pocket depth �93 3 mm at the tooth/teeth to be treated
  • No tooth mobility (mobility grade �91)
  • No cervical composite restorations or non-carious cervical lesions
  • Presence of a shallow vestibule (<5 mm)
Not Eligible

You will not qualify if you...

  • Pregnancy or lactation
  • Untreated periodontal disease
  • Presence of parafunctional habits
  • Poor oral hygiene (full-mouth plaque score >20%)
  • Malpositioned, rotated, or crowded teeth in the buccal position
  • Known systemic diseases (e.g., AIDS, diabetes mellitus)
  • Any condition or medication affecting gingival wound healing
  • ASA physical status classification III or higher

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Kahramanmaraş Sütçü İmam University

Kahramanmaraş, Kahramanmaraş, Turkey (Türkiye), 46000

Actively Recruiting

Loading map...

Research Team

E

esra bozkurt

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here