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Modified Sling and Conventional Suture Techniques in Free Gingival Graft Operations

B

Bezmialem Vakif University

Status

Completed

Conditions

Gingival Recession, Localized

Treatments

Procedure: Gingival unit graft and conventional suture technique
Procedure: Conventional graft and modified sling suture technique
Procedure: gingival unit graft+modified sling suture technique
Procedure: Conventional graft and conventional suture technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06197893
SSHAKILIYEVA

Details and patient eligibility

About

The aim of this study is to investigate the effects of conventional suture (CS) and modified sling suture (MSS) techniques, applied in free gingival graft (FGG) surgery using gingival unit graft (GUG) and conventional graft (CG) techniques, on clinical parameters and graft dimensions.

Full description

Background: The aim of this study is to investigate the effects of conventional suture (CS) and modified sling suture (MSS) techniques, applied in free gingival graft (FGG) surgery using gingival unit graft (GUG) and conventional graft (CG) techniques, on clinical parameters and graft dimensions.

METHODS: 52 individuals having Cairo Type 2 (RT2) and Type 3 (RT3) gingival recessions in mandibular anterior region were divided into four groups as a) GUG+MSS (n=13), b) GUG+CS (n=13), c) CG+MSS (n=13) and d) CG+CS (n=13). Keratinized gingival width (KGW), keratinized tissue thickness (KGT), relative gingival recession height (rGRH), and relative vestibule depth (rVD) measurements were recorded using a digital caliper and periodontal probe UNC 15. Dimensional changes (Δ) of the graft surface area (GSA) was determined by ImageJ software. All measurements were done at baseline and repeated 1st and 3rd months.

Enrollment

60 patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Systemically healthy individuals
  • <1 mm of attached gingiva on mandibular incisors
  • PI and GI scores <1
  • Patients who had not previously undergone soft tissue surgery in the relevant area

Exclusion criteria

  • Pregnant or lactating women
  • Patients younger than 18 years old
  • Mandibular incisors with having restoration, probing depth ≥ 3 mm, malposition and/or endodontic problem
  • Maxillary premolars with gingival recession in the palatal area and/or prosthetic restoration

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

60 participants in 4 patient groups

1. GUG+MSS
Experimental group
Description:
The GUG was obtained from the maxillary premolar area. The dissected graft was fixed to the recipient site using a modified sling suture technique.
Treatment:
Procedure: gingival unit graft+modified sling suture technique
2. GUG+CS
Experimental group
Description:
The GUG was obtained from the maxillary premolar area, as detailed experimental GUG+MSS group. The dissected graft was fixed to the recipient site using conventional suture technique.
Treatment:
Procedure: Gingival unit graft and conventional suture technique
3. CG+MSS
Experimental group
Description:
Conventional graft dimensions were determined with aluminum foil and the foil was placed in the palatial region at the level of the maxillary premolars, at least 2 mm away from the free gingival margin of the adjacent teeth. The dissected graft was fixed to the recipient site with 5/0 polypropylene suture using a modified sling suture technique, as detailed experimental GUG+MSS group.
Treatment:
Procedure: Conventional graft and modified sling suture technique
4. CG+CS
Experimental group
Description:
The dissected conventional graft, as detailed experimental CS+MSS group, fixed recipient bed with conventional suture technique, as detailed experimental GUG+CS group.
Treatment:
Procedure: Conventional graft and conventional suture technique

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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