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Clinical Trials in Egypt / NCT06435780
Recruiting Not applicable

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

NCT06435780 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2023-04-01
Last updated
2026-01-29

Condition(s) studied

Defect in Alveolar Ridge

Investigational drug(s) / intervention(s)

DIPRF

DIPRF: Denuded interpositional pedicled rolled flap technique

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: 1. Adults above the age of 18 to 50 years. 2. Males and females as confirmed by asking the female patients about whether they are pregnant or not 3. Patient's with Seibert classification class I requiring future rehabilitation of one or more premolar region and sound adjacent teeth. 4. Soft tissue thickness on the palatal tissues more than 6mm at the site of harvesting the graft. 5. Presence of Mandibular posterior teeth opposing the tooth to be replaced for occlusion. 6. Clinically healthy soft tissues with no signs of clinical pathology of the soft tissue. 7. Good oral hygiene. 8. Patient accepts to sign an informed consent. 9. ASA I or ASA II Patient. Exclusion Criteria: 1. Patients with ridge defects due to bone defect 2. Smoker patients who smoke more than 10 cigarettes per day 3. Pregnant females

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Misr International University Cairo Egypt Recruiting

More Misr International University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06435780 on ClinicalTrials.gov ↗ ← All trials in Egypt