Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
NCT06435780

Novel Technique Versus Conventional Subepithelial Connective Tissue Graft in Treatment of Ridge Contour Defects

Led by Misr International University · Updated on 2026-01-29

50

Participants Needed

1

Research Sites

195 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study is to clinically and radiographically evaluate and compare two techniques to augment soft tissues: the conventional subepithelial connective tissue graft technique and a novel denuded interpositional pedicled rolled flap technique (DIPRF) These techniques will be used to augment edentulous ridges that are recommended for rehabilitation by an implant or a fixed restoration.

CONDITIONS

Official Title

Novel Technique Versus Conventional Subepithelial Connective Tissue Graft in Treatment of Ridge Contour Defects

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 50 years
  • Male or female, with pregnancy status confirmed for females
  • Patients with Seibert class I soft tissue ridge defects in the premolar region requiring rehabilitation
  • Soft tissue thickness at the graft harvesting site greater than 6 mm
  • Presence of mandibular posterior teeth opposing the tooth to be replaced
  • Clinically healthy soft tissues without signs of pathology
  • Good oral hygiene
  • Patient agrees to sign informed consent
  • Patient classified as ASA I or ASA II
Not Eligible

You will not qualify if you...

  • Patients with ridge defects caused by bone defects
  • Smokers who consume more than 10 cigarettes daily
  • Pregnant women

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Misr International University

Cairo, Egypt

Actively Recruiting

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Research Team

H

Hebattallah A Mattar

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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