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3D VOLUMETRIC CHANGE OF THE PALATAL DONOR REGION IN WOUND HEALING

NCT06250179 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2024-07-25

No results posted yet for this study

Summary

The purpose of this clinical trial is planned to be conducted with 45 individuals aged between 18-65, with Cairo type I gingival recession and patients requiring free gingival surgery. It was aimed to investigate when the palatal mucosa will return to its previous volume in the donor area and the effect of smoking. The main questions it aims to answer are:

* Evaluation of 3D volume change of the palatal donor area from which free gingival graft was taken
* determining how long it takes for the palatal mucosa to regain its original shape and thickness Participants will be asked to comply with postoperative recommendations and pay attention to oral hygiene.

If there is a comparison group: Researchers use it to see if smoking affects the volume change in the donor area.

They will compare non-smokers with clinically healthy gums, 'light' smokers who report smoking less than 5 cigarettes per day and patients with clinically healthy gums, and ex-smokers with clinically healthy gums who have not smoked for 5 years.

Conditions

  • Free Gingival Graft Volume Change

Interventions

PROCEDURE

free gingiva graft surgery

For insufficient gingival height in patients, the free gingival graft taken from the palate will be sutured to the relevant area.

Sponsors & Collaborators

  • DİLEK ÖZKAN ŞEN

    collaborator UNKNOWN

  • Necmettin Erbakan University

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-07-10
Primary Completion
2024-09-01
Completion
2024-12-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06250179 on ClinicalTrials.gov