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Clinical Trials in Egypt / NCT06646432
Recruiting Not applicable

Treatment of Gingival Recession With Tunnel Technique Using Connective Tissue Graft and Injectable Platelet Rich Fibrin

NCT06646432 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2024-11-01
Last updated
2025-01-29

Condition(s) studied

Gingival Recession

Investigational drug(s) / intervention(s)

Tunnel with connective tissue graft and injectable platelet rich fibrinTunnel with connective tissue graft only

Tunnel with connective tissue graft and injectable platelet rich fibrin: Tunnel with connective tissue graft and injectable platelet rich fibrin

Tunnel with connective tissue graft only: Tunnel technique with connective tossue graft only without injectable platelet rich fibrin

Study summary

Gingival recession is a common periodontal problem. Consequences include teeth sensitivity, poor esthetics and impaired oral hygiene access. Mild cases are managed by optimizing oral hygiene measures, correction of any causative factor such as faulty tooth brushing, improper dental restoration or denture clasp. Prescription of desensitization products such as specific tooth gels or mouth washes can manage the sensitivity problem. Deeper recession defects need to be addressed by surgical procedures. Coronally advanced flap with connective tissue graft is the gold standard procedure. However, it has some drawbacks due to the need for papillary incisions and vertical incisions in some cases. Within the era of minimally invasive periodontology, tunnel technique with connective tissue graft showed results comparable to coronally advanced flap with connective tissue graft but with some limitations. Addition of another agent may enhance the results of tunnel technique. Injectable platelet rich fibrin is known for its content of growth factors and effects on soft tissue healing. Aim: The study aim is to compare the surgical management of gingival recession with tunnel technique using connective tissue graft and injectable platelet rich fibrin to tunnel with connective graft without injectable platelet rich fibrin.

Methodology: 30 patients with miller class I or II gingival recession will be enrolled. 15 in the test group (Tunnel+ CTG+ i-PRF) and 15 in control group (Tunnel+ CTG). Clinical evaluation at 6 months

Eligibility

Sex
ALL
Min age
21 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * More than 21 years old * Systemically healthy * Presence of Miller class I/II gingival recession * Presence of identifiable CEJ Exclusion Criteria: * Smoking * Systemic disease that contraindicates surgical procedures. * Poor compliance with oral hygiene measures * Necrotizing gingival conditions * Ongoing active periodontitis

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of dentistry, Suez canal university Ismailia Egypt Recruiting

More Suez Canal 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 NCT06646432 on ClinicalTrials.gov ↗ ← All trials in Egypt