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NOT YET RECRUITING
NCT07876921
NA

MEBO Bio-Dressing on Patient-Reported Outcomes and Tissue Healing Following Rotary Gingival Depigmentation

Sponsor: Cairo University

View on ClinicalTrials.gov

Summary

The purpose of this randomized, single-blind, parallel-group clinical trial is to evaluate the clinical efficacy of Moist Exposed Burn Ointment (MEBO) as a biological topical dressing compared to open secondary healing (no dressing) following rotary gingival depigmentation in adult patients. The study aims to investigate whether the application of MEBO reduces postoperative pain intensity, decreases rescue analgesic reliance, accelerates soft-tissue wound healing, and improves oral health-related quality of life over a 1-month follow-up period.

Official title: Rethinking Postoperative Care In Esthetic Periodontics: Effect of MEBO Bio-Dressing on Patient-Reported Outcomes and Tissue Healing Following Rotary Gingival Depigmentation: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 50 Years

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2026-11

Completion Date

2027-01

Last Updated

2026-10-15

Healthy Volunteers

No

Interventions

DRUG

MEBO Ointment

Topical lipid-based ointment applied directly over the de-epithelialized gingival wound immediately post-surgery and re-applied topically by the patient 3 times daily for 7 days.

Locations (1)

Faculty of Dentistry, Cairo University

Cairo, Cairo Governorate, Egypt