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Clinical Trials/NCT06615687
NCT06615687
Not yet recruiting
Not Applicable

Inverted T-shape Free Gingival Graft Versus Free Gingival Graft for Treatment of RT2/RT3 Gingival Recession Defects : a Randomized Clinical Trial

Cairo University1 site in 1 country34 target enrollmentOctober 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gingival Recession
Sponsor
Cairo University
Enrollment
34
Locations
1
Primary Endpoint
Recession depth.
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The aim of this study is to compare the use of T-inverted shape Free Gingival Graft with Free Gingival Graft for improving the clinical attachment, gain partial root coverage, and improve Keratinized tissue width in recession type 2 /recession type 3 gingival recession defects .

Research question : In patients with RT2 / RT3 mandibular defects will the use of inverted T-shape free gingival graft differ from free gingival graft in Recession depth?

Registry
clinicaltrials.gov
Start Date
October 2024
End Date
August 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dina Galal Fouad Mohamed Hafeez

Principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients with RT2/RT3 gingival recession.
  • Indication for FGG treatment at mandibular incisor area (i.e., difficulty or discomfort during oral hygiene; gingival margin mobility; high muscle attachment and/or frenum pull; shallow vestibule and gingival recession.
  • KT width (KTW) \< 2 mm.
  • Ages 18-40 years old.
  • Patients with healthy systemic condition (Brightman. 1994).
  • Gingival and plaque index \<
  • Good oral hygiene (Wiesner et al. 2010).
  • Accepts 6 months follow-up period (cooperative patients)

Exclusion Criteria

  • Poor oral hygiene.
  • Patient with a physical disability that hinders the upkeep of good oral hygiene measures.
  • Intake of any medications known to affect gingival homeostasis or to interfere with wound healing.
  • Pregnant or lactating women.
  • RT1 gingival recession.
  • Caries or non-carious cervical lesions at recipient sites.
  • Severely malpositioned teeth.
  • Teeth with residual probing depth ≥ 4 mm.
  • Mobility ≥ 1 mm.
  • Pervious periodontal surgery within the last 6 months before the start of the trial.

Outcomes

Primary Outcomes

Recession depth.

Time Frame: baseline, 1 month , 3 months and 6 months

Will be measured as the distance from the CEJ to the most apical extension of the gingival margin.

Secondary Outcomes

  • Width of keratinized gingiva .(baseline, 1 month , 3 months and 6 months)
  • Recession width(baseline, 1 month , 3 months and 6 months)
  • Gingival thickness(baseline, 1 month , 3 months and 6 months)
  • Root coverage esthetic score(baseline, 1 month , 3 months and 6 months)
  • The Distance between the contact point and the top of the papilla (DCP).(baseline, 1 month , 3 months and 6 months)
  • Probing Depth(baseline, 1 month , 3 months and 6 months)
  • Gingival Index(baseline, 1 month , 3 months and 6 months)
  • Plaque Index(baseline, 1 month , 3 months and 6 months)

Study Sites (1)

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