AzTrials
AzTrials

Gingival Recession, Mucogingival SurgeryNCT07706257

Gingival Unit Graft Versus Free Gingival Graft: 18-Month Digital Color Analysis

An observational study of Gingival Recession, Mucogingival Surgery and Keratinized Tissue Deficiency, run by Bezmialem Vakif University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this retrospective clinical study is to compare the long-term aesthetic integration and clinical outcomes of two periodontal plastic surgery techniques: Gingival Unit Grafting (GUG) and Free Gingival Grafting (FGG). Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Gingival Unit Grafting and Conventional Free Gingival Grafting
Type of treatment
Surgery or procedure
How many people
40 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Mar 2022to 31 Dec 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: The study population consists of adult patients seeking treatment for localized gingival recessions on mandibular incisors at a university faculty of dentistry.

Who may be able to join

  • Systemically healthy individuals aged between 18 and 65 years
  • No systemic diseases contraindicating periodontal surgery
  • Not taking medications known to exert adverse effects on periodontal tissues
  • Presenting with Cairo Type 2 (RT2) or Type 3 (RT3) localized gingival recessions on mandibular incisors
  • Presence of ≤1 mm of attached gingiva resulting in difficulty maintaining plaque control
  • Full-mouth plaque and gingival index scores ≤1
  • Bleeding on probing (BOP) <10%
  • No history of prior soft tissue surgery in the designated area

Who cannot join

  • Individuals who are pregnant or lactating.
  • Presenting with gingival recession or prosthetic restorations at the donor site (maxillary premolar palatal region).
  • Cases demonstrating caries, abrasions, or restorations on the root surfaces of the related teeth.
  • Individuals with known allergies to dental impression materials.
  • Periodontal pocket depth greater than 3 mm.
  • Tooth malposition.
  • Endodontic complications.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Bezmialem Vakif University, Faculty of Dentistry

    Istanbul, Fatih, 34093

Other trials in Turkey (Türkiye)

About this study

Official title: Clinical Outcomes and Digital Color Stability of Gingival Unit Graft Versus Free Gingival Graft: An 18-Month Comparative Digital Photographic Color Analysis Study

The purpose of this retrospective clinical study is to compare the long-term aesthetic integration and clinical outcomes of two periodontal plastic surgery techniques: Gingival Unit Grafting (GUG) and Free Gingival Grafting (FGG). The study evaluates the effectiveness of these procedures in increasing keratinized tissue width and assesses the color integration of the grafted tissues with the surrounding gingiva over an 18-month follow-up period using objective digital color analysis based on CIE Lab and RGB parameters.

Read the detailed description

This single-center retrospective study included patients treated with either Gingival Unit Grafts (GUG) or Free Gingival Grafts (FGG) for the management of Cairo Type 2 and Type 3 gingival recessions between March 2022 and December 2022. Clinical and photographic records obtained at baseline and during follow-up visits up to 18 months were retrospectively analyzed. The primary outcome was the evaluation of color integration of the grafted tissues using objective digital color analysis based on CIE Lab and RGB parameters. Secondary outcomes included changes in keratinized tissue width. The aim of the study was to compare the long-term aesthetic integration and clinical performance of GUG and FGG and to determine which technique provides superior color matching with the surrounding tissues.

Being tested
Gingival Unit Grafting, Conventional Free Gingival Grafting
Keywords
Gingival Unit Graft, Free Gingival Graft, Aesthetics, Digital color analysis, Color matching
Medical subject headings
Gingival Recession

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Gingival Unit GraftingProcedure or surgery

    Harvesting a gingival unit graft and transplanting it to the recipient area to increase keratinized tissue width and assess long-term aesthetic integration.

  • Conventional Free Gingival GraftingProcedure or surgery

    Harvesting a conventional free gingival graft and transplanting it to the recipient area to increase keratinized tissue width and serve as a control group for aesthetic integration.

Study groups in NCT07706257
Study groupRoleWhat they receive
Gingival Unit Graft (GUG) GroupPatients who underwent periodontal plastic surgery using Gingival Unit Grafts for keratinized tissue gain
Receives: Procedure: Gingival Unit Grafting
Conventional Free Gingival Graft (FGG) GroupPatients who underwent periodontal plastic surgery using Conventional Free Gingival Grafts for keratinized tissue gain
Receives: Procedure: Conventional Free Gingival Grafting

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Aesthetic Integration (Color Evaluation)

    Objective assessment of color integration between the grafted tissue and the surrounding gingiva using digital color analysis. Color parameters were evaluated based on the CIE Lab* color space system and RGB color channels obtained from standardized clinical photographs. The degree of color matching between grafted and adjacent tissues was assessed over the follow-up period.

    Measured: Baseline and 18 months post-surgery

Secondary outcomes (1)
  1. Keratinized Tissue Width (KTW)

    The clinical measurement of the width of keratinized tissue in millimeters, evaluated from the gingival margin to the mucogingival junction using a standard periodontal probe to determine the amount of tissue gain.

    Measured: Baseline and 18 months post-surgery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jul 2026
  2. Study start1 Mar 2022
  3. Primary completion30 Jun 2024
  4. Study completion31 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Retrospective
Enrolment
40 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07706257
Sponsor's protocol ID
No: 2024/304
Status last verified
Jul 2026
First submitted
11 Jul 2026
Last updated
16 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Gingival Recession, Mucogingival Surgery and Keratinized Tissue Deficiency, run by Bezmialem Vakif University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 16 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Aesthetic Integration (Color Evaluation) (time frame: Baseline and 18 months post-surgery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Jul 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in