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Efficacy of PRF in Hypospadias Repair

Evaluating the Efficacy of Platelet-Rich Fibrin (PRF) in Hypospadias Repair: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07757828
Enrollment
80
Registered
2026-08-11
Start date
2026-08-01
Completion date
2027-10-01
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypospadias

Keywords

Hypospadias, PRF, Repair

Brief summary

Hypospadias is an anomaly characterized by an ectopic ventral urethral meatus, and an incomplete or hooded prepuce. Its incidence is estimated at 1 in 200-300 live male births, with variations across populations and severity types. Successful hypospadias repair depends largely on optimal tissue healing and robust vascular support around the neourethra. Thus, many adjunctive techniques have been investigated to improve outcomes, including dartos flaps, tunica vaginalis flaps, and various tissue sealants. In recent years, attention has turned toward biological augmentation strategies, particularly the use of platelet-rich plasma (PRP) and platelet-rich fibrin as a potential enhancer of wound healing. Platelet-rich fibrin (PRF), a second-generation autologous platelet concentrate, has recently emerged as another promising biologic in tissue engineering. This study aims to evaluate the effect of PRF application in primary hypospadias repair surgery and determine its effect in improving healing and reduction of postoperative complications.

Detailed description

All patients included in the study will undergo primary hypospadias repair using the standardized Tubularized Incised Plate (TIP) urethroplasty technique (Snodgrassi procedure), under general anesthesia and by the same surgical team to minimize variability * Steps of the Surgical Procedure (Same for Both Groups): 1\. Preoperative preparation: * IV antibiotics, sterile field setup, general anesthesia. 2. Urethral plate incision and tubularization over a 6-8 Fr stent using absorbable sutures. 3\. application of PRF (Group A only): * 8-10 mL of autologous blood is drawn into plain (non-anticoagulant) tubes according to the patient's weight and the size of the patch needed. * The sample is immediately centrifuged using the single-spin method (typically 3,000 rpm (400x g) for 12 minutes). * This produces three layers: * Top layer: acellular plasma (PPP) * Middle layer: platelet-rich fibrin (PRF) clot * Bottom layer: red blood cells The PRF clot is gently removed and compressed using a gauze to form a thin PRF membrane. * PRF membrane is fixed on top of the suture line as a first layer and under the incision line as a second layer and secured using a few resorbable polyglyconate 6/0 interrupted sutures. 4\. Glansplasty and skin closure using standard techniques in both groups 5. Catheter and dressing: * A soft catheter is left in place for 5-7 days. * A mild compression dressing is applied.

Interventions

PROCEDURETubularized Incised Plate urethroplasty with intraoperative placement of autologous PRF onto the urethral plate.

Urethral plate incision and tubularization over a 6-8 Fr stent using absorbable sutures. Application of PRF where 8-10 mL of autologous blood is drawn into plain (non-anticoagulant) tubes and a thin PRF membrane is extracted which is fixed on top of the suture line as a first layer and under the incision line as a second layer and secured using a few resorbable polyglyconate 6/0 interrupted sutures. Glansplasty and skin closure using standard techniques and fixing catheter and dressing

PROCEDUREstandard Tubularized Incised Plate urethroplasty

Urethral plate incision and tubularization over a 6-8 Fr stent using absorbable sutures. Glansplasty and skin closure using standard techniques and fixing catheter and dressing

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

All patients included in the study will undergo primary hypospadias repair using the standardized Tubularized Incised Plate (TIP) urethroplasty technique (Snodgrassi procedure), under general anesthesia and by the same surgical team to minimize variability

Eligibility

Sex/Gender
MALE
Age
6 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed with primary distal or mid-penile hypospadias. * Eligible for first-time (primary) surgical repair using the TIP (Tubularized Incised Plate) technique.

Exclusion criteria

* previous hypospadias surgery. * Associated severe chordee requiring staged repair or patient with crippled hypospadias. * Children with systemic diseases that may impair wound healing (e.g., diabetes, immunodeficiency, malnutrition). * Presence of bleeding or coagulation disorders. * Medically Unfit for surgery.

Design outcomes

Primary

MeasureTime frameDescription
Urethrocutaneous fistula formation6 monthsIncidence of urethrocutaneous fistula formation
Parental satisfaction Assessment6 monthsParental satisfaction assessed using a standardized questionnaire HOPE score

Countries

Egypt

Contacts

CONTACTMahmoud Mohamed Magdy El-Ansary, MSc
mahmoudmagdy99@hotmail.com+201114393349
CONTACTYounan R. Samir, M.D.
dr_yona@live.com+201201255511
STUDY_CHAIRHany H. Gad, Professor

Ain Shams University

STUDY_DIRECTORHossam M.H. ElAwady, Professor

Ain Shams University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026