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Local Oestrogen Versus Placebo as Preoperative Treatment in Patients With Severe Hypospadias: Effects on Post-operative Complications

Local Oestrogen Versus Placebo as Preoperative Treatment in Patients With Severe Hypospadias: Effects on Post-operative Complications.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01370798
Acronym
HYPOSPADES
Enrollment
244
Registered
2011-06-10
Start date
2011-05-26
Completion date
2017-09-18
Last updated
2025-09-04

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

Conditions

Hypospadias

Keywords

Severe hypospadias, local oestrogen, promestriene, Onlay-tube-onlay urethroplasty, post-operative complications, fistula dehiscence

Brief summary

Hypospadias is a congenital abnormality of the penis that is caused by incomplete development of the anterior urethra. This pathology is one of the most common genital anomalies in paediatric urology .The incidence is reported to be 1 out of 250 live male births and is increasing regularly. The hypospadias surgeries present a high risk of post operative complications requiring re-interventions. A great part of the post operative complications is related to imperfect healing issues. If androgen stimulation seems to be deleterious, at the opposite, oestrogen could impact positively on the skin healing process. This point leads to the hypothesis that local transcutaneous oestrogen stimulation on the ventral and dorsal penile faces decreases the number of skin healing post-operative defects. The objective of the study is to assess the effect of oestrogen (applied once daily for 2 months prior to surgery) on the post-operative complications.

Interventions

Promestriene cream 1%, 1g per day during 2 months, cutaneous application

DRUGPlacebo

Placebo of promestriene cream, 1g per day during 2 months, cutaneous application

PROCEDUREUrethroplasty

Onlay-tube-onlay urethroplasty performed by a physician expert of this technique (at least 5 years of practical ability)

RADIATIONWrist X ray

Wrist X ray to follow the degree of bone maturation

PROCEDUREBlood test

Hormonal dosage: Oestradiol, testosterone, FSH-LH and AMH

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
9 Months to 36 Months
Healthy volunteers
No

Inclusion criteria

* Severe hypospadias with a division of the corpus spongiosum behind the midshaft of the penis and for which repair requires a urethral substitution by onlay urethroplasty. * Subjects operated between 9 and 36 months old. * Subjects operated in one of the departments of paediatric urology involved in the study. * Surgery performed by a surgeon with at least 5 years of practical experience in the hypospadias surgery. * Written informed consent obtained from parents or legal guardians prior to the participation to the study * All hypospadias aetiology (hormonal, karyotype or genetic)

Exclusion criteria

* Refusal to participate * Subjects with glandular hypospadias * Subjects aged \<9 months or \> 36months old at time of surgery. * Subjects who had prior surgery of penis (circumcision or hypospadias surgery) * Subjects treated with androgens (Human Chorionic Gonadotrophin or delayed testosterone) within 6 months prior to surgery. * Intolerance to promestriene or its excipients. * Not affiliated to a healthy or social security cover. * Known tumoral risk * Pure or mixed gonadal dysgenesis (45, X0/46,XY)

Design outcomes

Primary

MeasureTime frame
Number of patient with postoperative urethral fistula and dehiscence1 year

Secondary

MeasureTime frameDescription
post-surgical complications1 yearTotal number and type of post-surgical complications
Re-intervention not related to wound healing1 yearNumber of re-interventions not related to wound healing
Re-intervention related to wound healing1 yearNumber of re-interventions for fistula or dehiscence not related to stenosis, in the first year post surgery.
Bone age evaluation14 monthesHand and wrist radiography at inclusion and 1 year after surgery.
Clinical tolerance of the treatment14 monthsNumber and type of adverse events
Hormone measurement2 monthsPlasmatic concentrations of Oestradiol, Testosterone, LH, FSH at inclusion and at 2 months (at the end of study treatment)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026