CClinicalTrials.gg
CompletedNCT04605068DuckettvDFPFUpdated Oct 27, 2020

Transverse Preputial Island Flap Versus Double Faced Preputial Flap for Repair of Penoscrotal Hypospadias With Chordee

An interventional study of Transverse preputial island flap (Duckett's technique) and Double-faced preputial flap (DFPF) in Hypospadias, Penoscrotal and Chordee, sponsored by dr. Muhammad Abdelhafez Mahmoud, MD. Completed. Open to male participants aged 6 Months to 14 Years. Per ClinicalTrials.gov, last updated 2020-10-27.

Sponsored by dr. Muhammad Abdelhafez Mahmoud, MD · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 years 7 months after the study started (first participant enrolled Mar 2014, registered Oct 2020).
Phase
Not applicable
Study type
Interventional
Enrollment
144
Allocation
Randomized
Ages
6 Months to 14 Years
Sex
Male
01

Study summary

The purpose of this study is to compare the outcomes and complications of the transverse preputial island flap (Duckett's procedure) to those of double-faced preputial flap (DFPF) for one-stage repair of penoscrotal hypospadias with chordee, in addition to clinical functional evaluation by estimated urine flow.

Read the detailed description

Type of study: RCT

Review of literature:

  • Different modalities of urethroplasty for repair of proximal hypospadias with chordee (two-stage repair, one-stage repair, flap, graft).
  • Disadvantages of two-stage urethroplasty for proximal hypospadias with chordee..
  • Merits of one-stage urethroplasty for proximal hypospadias with chordee. This is a prospective randomized controlled study conducted at pediatric surgery department, Al-Houssain \& New Damietta Al-Azhar University Hospitals, from March 2014 to March 2020, on 144 male patients with penoscrotal hypospadias with chordee. Patients will be investigated by routine laboratory tests for fitness for surgery. All of them will undergo one-stage repair using either of 2 techniques of tubularized preputial flap; Duckett's versus DFPF. Written informed consent will be obtained from parents of all participants in the study.

Institutes of the study:

A multicenter study at Pediatric Surgery Departments, Al-Azhar University hospitals in Cairo and New Damietta. Number of cases: One-hundred-Forty four male patients. Time frame: period of 6 years.

Ethical Consideration:

The protocol will be discussed and approved for clinical study by the Ethical Research Committee at the principal investigator's hospital. The procedures and the aim of the study will be clearly explained to the patient and the family. A written informed consent will be obtained before enrollment of the patients into the study. The family refusal to give consent for one-stage repair is respected but does not deprive the patient from getting surgical care by two-stage repair.

Preoperative preparation:

All patients will be subjected to history taking, clinical examination, and necessary laboratory investigations (CBC, Coagulation profile, Liver and Renal Function tests, Electrolytes Panel, Urinalysis). They will receive a dose of single broad-spectrum antibiotic 30 min-1 hour before surgery. Patients will be randomly divided (using the computer-generated randomization table) into two equal groups, each will include 72 patients; Group I will undergo transverse preputial island flap (Duckett's technique) and Group II will undergo double-faced preputial flap (DFPF). Both techniques will be done by all members of the surgical team equally.

Follow-up:

Patients will be followed-up at OPD.

Statistical Analysis:

Data were collected using a data collecting sheets (annexes) and were analyzed using the statistical package for social sciences (SPSS) version 24.0 (IBM SPSS Statistics for Windows, IBM Corp, Armonk, NY, USA). Continuous variables were expressed as mean±standard deviation (SD), range, and average and categorical variables were expressed as frequency count \& percentage. Fisher's exact test was used for comparison of frequency counts/percentage. A two-sided p-value \< 0.05 was considered statistically significant.

Discussion:

It will focus on one-stage urethroplasty using the preputial flap for proximal hypospadias with chordee. The results obtained from this study will be compared between both group and with those reported in the literature.

Also, it will focus on results, complications, their management, and clinical evaluation by estimated urine caliber and micturition time. At the end, the investigators will conclude the reconstructive technique that gives the better results and least morbidity.

02

Conditions studied

  • Hypospadias, Penoscrotal
  • Chordee

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Keywords

  • Penoscrotal Hypospadias
  • Chordee
  • Tubularized Double-Faced Preputial Flap
  • Duckett's Urethroplasty
  • One-Stage Repair
03

In context

Hypospadias

131 studies on the registry are indexed under Hypospadias; 34 are open to participants now.

This study's enrollment of 144 is above the median of 68 across 102 interventional studies indexed under Hypospadias.

Browse Hypospadias studies →

Lead sponsor

dr. Muhammad Abdelhafez Mahmoud, MD is the lead sponsor of 8 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 14 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • Uncircumcised male patients with penoscrotal hypospadias,
  • rudimentary urethral plate
  • with moderate-to-severe chordee and
  • no history of previous repair

Exclusion criteria

Exclusion Criteria:

  • circumcised patients,
  • patients with other types of hypospadias such as glanular or distal shaft or
  • with mild chordee corrected after penile degloving,
  • recurrent hypospadias, or
  • lost to follow-up.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
144 participants (actual)

Study arms

  • Active comparator
    Transverse preputial island flap (Duckett's technique)

    72 patients (Group I) with penoscrotal hypospadias with chordee

    Procedure: Transverse preputial island flap (Duckett's technique)

  • Active comparator
    Double-faced preputial flap (DFPF)

    72 patients (Group II) with penoscrotal hypospadias with chordee

    Procedure: Double-faced preputial flap (DFPF)

Interventions

  • ProcedureTransverse preputial island flap (Duckett's technique)
  • ProcedureDouble-faced preputial flap (DFPF)
06

What researchers measure

Primary outcomes

  1. Urethrocutaneous fistula (number & percent)

    Urethrocutaneous fistula

    Time frame: 2 years

  2. Meatal stenosis (number & percent)

    Meatal stenosis

    Time frame: 2 years

  3. Urethral stricture (number & percent)

    Urethral stricture

    Time frame: 3 years

Secondary outcomes

  1. Penile rotation (number & percent)

    Penile rotation

    Time frame: 3 years

  2. Urine stream (in caliber)

    Urine stream

    Time frame: 3 years

  3. Urine stream (in meters)

    Urine stream

    Time frame: 3 years

  4. Micturition time (in seconds)

    Micturition time

    Time frame: 3 years

  5. Follow-up period (in months)

    Follow-up period

    Time frame: 5 years

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Yes — Data will be available for other researchers including methodology, figures, tables, results, and philosophy of discussion and the value this study will add to the literature

Supporting information: Study protocol, Sap, Icf

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 27, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04605068
Lead sponsor
dr. Muhammad Abdelhafez Mahmoud, MD
Responsible party
dr. Muhammad Abdelhafez Mahmoud, MD (Lecturer of pediatric surgery, Al-Azhar University) — Sponsor-investigator
First posted
Oct 27, 2020
Start date
Mar 2014
Primary completion
Sep 2019
Completion
Mar 2020
Last update
Oct 27, 2020

Study contacts

Mohamed M Shahin, MD
principal investigator · Al-Azhar New Damietta University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2020. You cannot join it, but the record below documents what was studied.

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