CClinicalTrials.gg
Not yet recruitingNCT07404722Updated Feb 11, 2026

Urethral Plate Flap vs. Tunica Vaginalis Flap for Residual Severe Ventral Curvature in Hypospadias

An interventional study of Urethral Plate Flap Corporoplasty and Tunica Vaginalis Flap Corporoplasty in Residual Severe Ventral Curvature, Transection of the Urethral Plate and Corporoplasty, sponsored by The Children's Hospital of Zhejiang University School of Medicine. Not yet recruiting at 1 site in China. Open to male participants aged 6 Months to 14 Years. Per ClinicalTrials.gov, last updated 2026-02-11.

Sponsored by The Children's Hospital of Zhejiang University School of Medicine · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
90
Allocation
Randomized
Ages
6 Months to 14 Years
Sex
Male
01

Study summary

The correction of ventral curvature in hypospadias follows a stepwise principle. Clinically, in some cases of hypospadias, residual severe ventral curvature (VC ≥ 30°) persists even after thorough skin degloving and transection of the urethral plate, due to the unbalanced development of the ventral and dorsal tunica albuginea of the corpus cavernosum. In such cases, ventral tunica albuginea incision and corporoplasty with a graft are mandatory.

Although the currently commonly used pedicled Tunica Vaginalis Flap (TVF) corporoplasty can effectively correct the curvature, it requires additional dissection of the scrotum and tunica vaginalis sac. This prolongs the operative time and poses risks of donor-site complications, such as testicular retraction and scrotal hematoma.

The novel Urethral Plate Flap (UPF) corporoplasty utilizes local pedicled urethral plate tissue for homologous repair. This study adopts a prospective, single-center, randomized, controlled, double-blind, non-inferiority trial design, enrolling 90 subjects. The aim is to verify that the therapeutic efficacy of the UPF technique in correcting such residual severe ventral curvature is non-inferior to that of TVF, while demonstrating significant advantages in surgical efficiency and donor-site safety.

This study aims, through a single-center, double-blind, RCT design, and under the strict indication of "residual severe ventral curvature after urethral plate transection," to verify efficacy via a "non-inferiority" hypothesis, and to verify safety and efficiency via a "superiority" hypothesis. The goal is to provide Level I evidence for the update of hypospadias guidelines, while simultaneously exploring the establishment of postoperative imaging evaluation standards.

02

Conditions studied

  • Residual Severe Ventral Curvature
  • Transection of the Urethral Plate
  • Corporoplasty
  • Pedicled Tunica Vaginalis Flap (TVF)
  • Novel Urethral Plate Flap (UPF)
  • Hypospadias

Browse trials for

03

In context

Hypospadias

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

This study's planned enrollment of 90 is above the median of 68 across 102 interventional studies indexed under Hypospadias.

Browse Hypospadias studies →

Lead sponsor

The Children's Hospital of Zhejiang University School of Medicine is the lead sponsor of 68 studies on the registry; 51 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

  • Age: 6 months to 14 years.
  • Diagnosis: Primary hypospadias (no history of prior hypospadias repair).
  • Intraoperative Condition: Residual ventral curvature ≥ 30° confirmed by artificial erection test after transection of the urethral plate.
  • Consent: Signed informed consent provided by the participant's legal guardian.

Exclusion criteria

Exclusion Criteria:

① Glans diameter \< 1 cm; ② Combined with cryptorchidism; ③ Combined with severe bleeding disorders or coagulation dysfunction.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
90 participants (estimated)

Study arms

  • Experimental
    Urethral Plate Flap Corporoplasty

    1. After degloving and transecting the urethral plate, mobilize the urethral plate. 2. Transect the tunica albuginea at the point of maximal curvature to fully correct the ventral curvature. 3. Mobilize and open the tunica vaginalis sac, and harvest a pedicled Tunica Vaginalis Flap (TVF). 4. Transfer the TVF to the ventral side to repair the tunica albuginea defect, and suture with 6-0 absorbable sutures. 5. Mobilize the space between the scrotal skin and dartos fascia. Place 2 interrupted sutures between the external spermatic fascia near the testis and the dartos fascia at the scrotal base to fix the testis within the sub-dartos space.

    Procedure: Urethral Plate Flap Corporoplasty

  • Active comparator
    Tunica Vaginalis Flap Corporoplasty

    1. After degloving and transecting the urethral plate, mobilize the urethral plate. 2. Transect the tunica albuginea at the point of maximal curvature to fully correct the ventral curvature. 3. Mobilize and open the tunica vaginalis sac, and harvest a pedicled Tunica Vaginalis Flap (TVF). 4. Transfer the TVF to the ventral side to repair the tunica albuginea defect, and suture with 6-0 absorbable sutures. 5. Mobilize the space between the scrotal skin and dartos fascia. Place 2 interrupted sutures between the external spermatic fascia near the testis and the dartos fascia at the scrotal base to fix the testis within the sub-dartos space.

    Procedure: Tunica Vaginalis Flap Corporoplasty

Interventions

  • ProcedureUrethral Plate Flap Corporoplasty

    1.After degloving and transecting the urethral plate, mobilize the urethral plate. 2.Transect the tunica albuginea at the point of maximal curvature to fully correct the ventral curvature. 3.Mobilize and open the tunica vaginalis sac, and harvest a pedicled Tunica Vaginalis Flap (TVF). 4.Transfer the TVF to the ventral side to repair the tunica albuginea defect, and suture with 6-0 absorbable sutures. 5.Mobilize the space between the scrotal skin and dartos fascia. Place 2 interrupted sutures between the external spermatic fascia near the testis and the dartos fascia at the scrotal base to fix the testis within the sub-dartos space.

  • ProcedureTunica Vaginalis Flap Corporoplasty

    1.After degloving and transecting the urethral plate, mobilize the urethral plate. 2.Transect the tunica albuginea at the point of maximal curvature to fully correct the ventral curvature. 3.Mobilize and open the tunica vaginalis sac, and harvest a pedicled Tunica Vaginalis Flap (TVF). 4.Transfer the TVF to the ventral side to repair the tunica albuginea defect, and suture with 6-0 absorbable sutures. 5.Mobilize the space between the scrotal skin and dartos fascia. Place 2 interrupted sutures between the external spermatic fascia near the testis and the dartos fascia at the scrotal base to fix the testis within the sub-dartos space.

06

What researchers measure

Primary outcomes

  1. Recurrence Rate of Ventral Curvature at 12 Months Postoperatively

    Recurrence of ventral curvature is defined as residual ventral curvature ≥ 10° on lateral photographs during artificial erection.

    Time frame: 12 Months Postoperatively

Secondary outcomes

  1. Operative Time for Curvature Correction

    Recorded as the time from the "incision of the tunica albuginea" to the "completion of tunica albuginea repair and confirmation of a straight penis" (in minutes). This metric specifically excludes the time taken for urethroplasty and penile skin reconstruction to minimize confounding factors.

    Time frame: Intraoperative

  2. Incidence of Donor-Site Complications

    Assessment of complications related to the graft harvest site, including: Testicular events: Postoperative testicular retraction/ascent (defined as the testis position being higher than the middle of the scrotum). Scrotal events: Scrotal hematoma, edema, and secondary infections caused by these conditions.

    Time frame: From enrollment to the end of treatment at 12 months

  3. Continuity of the tunica albuginea

    Evaluation is performed by a sonographer blinded to group allocation using High-Frequency Penile Ultrasound Evaluation Evaluation Parameters: Continuity of the tunica albuginea (Categorized as: Continuous / Interrupted).

    Time frame: 12 months postoperatively

  4. Echogenicity of the corpus cavernosum beneath the graft

    Evaluation is performed by a sonographer blinded to group allocation using High-Frequency Penile Ultrasound Evaluation Evaluation Parameters: Echogenicity of the corpus cavernosum beneath the graft (Assessed for consistency with the host cavernous tissue)

    Time frame: 12 month postoperatively

07

Study locations

1 site
  • Children's hospital, Zhejiang University School of Medicine
    Hangzhou, Zhejiang 310052, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 11, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07404722
Lead sponsor
The Children's Hospital of Zhejiang University School of Medicine
Responsible party
Wei Ru (Associate Chief Physician, The Children's Hospital of Zhejiang University School of Medicine) — Principal investigator
First posted
Feb 11, 2026
Start date
Feb 23, 2026 (estimated)
Primary completion
Nov 30, 2027 (estimated)
Completion
Feb 22, 2029 (estimated)
Last update
Feb 11, 2026

Study contacts

Wei Ru Associate Chief Physician, MD
Contact
ruwei@zju.edu.cn
+86 13588064041

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion