Actively Recruiting

Phase Not Applicable
Age: 12Months - 10Years
MALE
ID07233265

Comparison of Single Incision Scrotal Orchidopexy Versus Standard Two Incision Inguinal Orchidopexy in Children With Palpable Undesended Testis in Children Hospital Faisalabad

Led by Children Hospital Faisalabad · Updated on 2025-11-24

60

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare two surgical methods for treating palpable undescended testis in male children under 10 years old. The study focuses on evaluating operative time, cosmetic outcomes, and post-operative complications to determine differences between the approaches. It is a randomized, interventional trial conducted at Children Hospital Faisalabad to assess these surgical techniques in young patients. Participants are randomly assigned to one of two groups. One group undergoes single incision scrotal orchidopexy, where the surgery is done through a single scrotal cut. The other group receives the standard two incision inguinal orchidopexy, involving separate cuts in the inguinal and scrotal areas. Both procedures are conventional orchidopexies aimed at repositioning the testis. During the study, children will be monitored for post-operative complications from 24 hours up to one month after surgery. Cosmetic outcomes will be evaluated two weeks post-surgery. The study includes follow-up visits to assess healing and surgical results, and all data will be collected to compare the two methods. Participation involves surgery, follow-up assessments, and monitoring for safety and effectiveness throughout the study period.

CONDITIONS

Brief Title

Comparison of Single Incision Scrotal vs Standard Two Incision Inguinal Orchidopexy in Children Under 10 Years.

Who Can Participate

Age: 12Months - 10Years
MALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Male children aged 1 month to 10 years
  • Palpable low-lying undescended testis
  • Consent obtained from parents or guardians
Not Eligible

You will not qualify if you...

  • Impalpable testis
  • Known bleeding disorder

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - 1 day

Participants undergo orchidopexy surgery through either a single scrotal incision or a standard two incision inguinal approach, followed by immediate post-operative care.

1 visit (in-person surgery and immediate recovery)

Post-operative Follow-up

Duration - Up to 1 month

Participants are monitored for post-operative complications and cosmetic outcomes after surgery.

Approximately 2 visits (in-person) including a visit around 2 weeks for cosmetic outcome assessment

Trial Site Locations

Total: 1 location

1

Children Hospital and Institute of Child Health Faisalabad

Faisalābad, Punjab Province, Pakistan

Actively Recruiting

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Research Team

I

Ijaz Ul Haq

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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