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Modified Sling and Conventional Suture Techniques in Free Gingival Graft Operations

Not Applicable
Completed
Conditions
Gingival Recession, Localized
Interventions
Procedure: Conventional graft and conventional suture technique
Procedure: Gingival unit graft and conventional suture technique
Procedure: gingival unit graft+modified sling suture technique
Procedure: Conventional graft and modified sling suture technique
Registration Number
NCT06197893
Lead Sponsor
Bezmialem Vakif University
Brief Summary

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.

Detailed 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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
60
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
4. CG+CSConventional graft and conventional suture techniqueThe dissected conventional graft, as detailed experimental CS+MSS group, fixed recipient bed with conventional suture technique, as detailed experimental GUG+CS group.
2. GUG+CSGingival unit graft and conventional suture techniqueThe 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.
1. GUG+MSSgingival unit graft+modified sling suture techniqueThe GUG was obtained from the maxillary premolar area. The dissected graft was fixed to the recipient site using a modified sling suture technique.
3. CG+MSSConventional graft and modified sling suture techniqueConventional 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.
Primary Outcome Measures
NameTimeMethod
Graft shrinkagebaseline, 1-, 3-months after FGG surgery

The shrinkage of the graft area was calculated according to the differences between the graft area at baseline, 1st, 3rd months using ImageJ software.

Secondary Outcome Measures
NameTimeMethod
Keratinized tissue weight gain (KTW)baseline, 1-, 3-months after FGG surgery

Alginate impressions of each participants were taken from mandibular teeth and an acrylic stent containing both mandibular canine-canine teeth was prepared. The measurements were made relatively with reference to the predetermined points on the stent. KTW was measured as the distance from the buccal midpoint of tooth between the free gingival margin and the alveolar mucosa.

Trial Locations

Locations (1)

Bezmialem Vakıf University

🇹🇷

Istanbul, Turkey

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