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Clinical Trials in Egypt / NCT07074717
Recruiting Not applicable

Penile Skin Versus Buccal Mucosal Graft in Augmentation Urethroplasty for Long Anterior Urethral Stricture

NCT07074717 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-01-01
Last updated
2025-07-20

Condition(s) studied

Penile SkinBuccal Mucosal GraftAugmentationUrethroplastyLong AnteriorUrethral Stricture

Investigational drug(s) / intervention(s)

Buccal Mucosal Graft (BMG) UrethroplastyPenile Skin Graft (PSG) Urethroplasty

Buccal Mucosal Graft (BMG) Urethroplasty: Urethroplasty using a buccal mucosal graft harvested from the inner cheek. The graft is dorsally onlaid to reconstruct the strictured urethral segment. The procedure is conducted under spinal or general anesthesia.

Penile Skin Graft (PSG) Urethroplasty: Urethroplasty using a penile skin graft harvested from the ventral surface of the penis. The graft is applied dorsally after excision of the fibrotic urethral segment. The surgery is performed under spinal or general anesthesia.

Study summary

The aim of this study is to analyze the outcomes of dorsal onlay buccal mucosal graft (BMG) and penile skin graft (PSG) urethroplasty in the management of long segment bulbar urethral stricture.

Eligibility

Sex
MALE
Min age
18 Months
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients with long segment anterior urethral stricture that was defined as a stricture with a length of more than 1 cm with spongiofibrosis. * Patients with previous failed urethral dilatation or direct vision internal urethrotomy (DVIU) Exclusion Criteria: * Patients with lichen sclerosus * Patients with history of hypospadias repair * Patients with recurrent urethral stricture after failed previous urethroplasty

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Tanta University Tanta El-Gharbia Governorate, Egypt Recruiting

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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 NCT07074717 on ClinicalTrials.gov ↗ ← All trials in Egypt