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Comparison of Cyanoacrylate Tissue Adhesive With Suture in the Treatment of Gingival Recession

NCT06499155 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-07-12

No results posted yet for this study

Summary

The aim of this randomized controlled clinical study was to determine the effects of gingival recession closure procedures performed with tissue adhesive and suture on gingival thickness, To evaluate the effect on the amount of gingival recession, keratinized tissue amount, clinical attachment level, probing pocket depth, papilla width and height, root coverage rate, wound healing, visual analogue scale, gingival index and plaque index.

The main questions it aims to answer are:

* Does the use of tissue adhesive in gingival recession closure procedures affect tissue healing in the recipient area?
* Does the use of tissue adhesive in gingival recession closure procedures affect tissue healing in the donor area? Participants will be informed about the study and the procedures to be performed, and the patients will continue their routine follow-up.

Conditions

  • Gingival Recession

Interventions

DEVICE

Use of periacryl in gingival recession closure procedures

Unlike the traditional procedure, periacryl tissue adhesive will be used in both the recipient and donor areas.

PROCEDURE

Use of sutures in gingival recession closure procedures

Both recipient and donor areas will be closed with traditional suturing techniques.

Sponsors & Collaborators

  • Necmettin Erbakan University

    lead OTHER

Principal Investigators

  • KEVSER YILDIRIM, RA · Necmettin Erbakan University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2024-07-15
Primary Completion
2024-12-15
Completion
2024-12-30
FDA Device
Yes

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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 NCT06499155 on ClinicalTrials.gov