Undescended TestisNCT07233265
Comparison of Single Incision Scrotal vs Standard Two Incision Inguinal Orchidopexy in Children Under 10 Years.
A study testing Single scrotal incision orchidopexy and Standard two incision inguinal orchidopexy in people with Undescended Testis, run by Children Hospital Faisalabad at 1 site in Pakistan.
Trial summary
This study compares the outcome of single incision scrotal orchidopexy with standard two incision inguinal orchidopexy in children under 10 years of age presented with palpable undesended tesis.The aim is to evaluate operative time,cosmetic outcome and post operative complications. Read more about this study
- Who is it for?
- Ages 12 months to 10 years, men only
- Conditions the study is for
- Undescended Testis
- What is being tested?
- Single scrotal incision orchidopexy and Standard two incision inguinal orchidopexy
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 sitePakistan
- Study dates
- Nov 2025to Jul 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 12 months to 10 years
- Men only
- No healthy volunteers
- Child
Who may be able to join
- Male children with age 1-10 years. Palpable low -lying undesended tesis.
Who cannot join
- Impalpable testis Known bleeding disorder
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Pakistan1 site, 1 recruiting
- Recruiting
Children Hospital and Institute of Child Health Faisalabad
Faisalābad, Punjab Province
Ijaz Ul Haq, 03305611906, ijazulhaq1995@gmail.com
Haq
About this study
Official title: Comparison of Single Incision Scrotal Orchidopexy Versus Standard Two Incision Inguinal Orchidopexy in Children With Palpable Undesended Testis in Children Hospital Faisalabad.
This study compares the outcome of single incision scrotal orchidopexy with standard two incision inguinal orchidopexy in children under 10 years of age presented with palpable undesended tesis.The aim is to evaluate operative time,cosmetic outcome and post operative complications.
Read the detailed description
All patients fulfilling the inclusion criteria admitted to paediatric surgery will be included by after taking informed consent from parents. Patients will be randomized in to two groups by lottery method.In group A ,orchidopexy is performed through single scrotal incision .In group B, orchidopexy is performed through standard two incision inguinal approach. This study compares the outcome interm of operative time, cosmetic outcome and post operative complications.
- Conditions
- Undescended Testis
- Being tested
- Single scrotal incision orchidopexy, Standard two incision inguinal orchidopexy
- Keywords
- Orchidopexy, Scrotal incision, Inguinal incision, Paediatric surgery
- Medical subject headings
- Cryptorchidism
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Single scrotal incision orchidopexyProcedure or surgery
Conventional orchidopexy performed through single scrotal incision
Standard two incision inguinal orchidopexyProcedure or surgery
Conventional orchidopexy performed through separate inguinal and scrotal incision
| Study group | Role | What they receive |
|---|---|---|
| Single scrotal incision orchidopexy | Experimental | Children in this group undergoes single incision scrotal orchidopexy with palpable undesended testis in superficial inguinal canal. Receives: Procedure: Single scrotal incision orchidopexy |
| Standard two incision inguinal orchidopexy | Active comparator | Children in this group undergoes standard two incision inguinal orchidopexy. Receives: Procedure: Standard two incision inguinal orchidopexy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Post operative complications
Numbers and type of post operative complications (Scrotal hematoma, infection, scrotal edema and testicular atrophy.
Measured: With in 24 hours -1month after surgery .
Secondary outcomes (1)
Cosmetic outcome
Cosmetic appearance of surgical scar assessed by standardized scale. Scale score range (1-10) lower score =better cosmetic outcome. Higher core = worse cosmetic outcome
Measured: 2 weeks after surgery
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Nov 2025
- Study startNov 2025 (estimated)
- Primary completionMay 2026 (estimated)
- Study completionJul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Undescended TestisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Children Hospital Faisalabad
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Ijaz Ul Haq, Children Hospital Faisalabad
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07233265
- Sponsor's protocol ID
- CH-FSD -Orchidopexy- 2025
- Status last verified
- Nov 2025
- First submitted
- 14 Nov 2025
- Last updated
- 24 Nov 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Single Incision Scrotal Orchidopexy Versus Standard Two Incision Inguinal Orchidopexy in Children With Palpable Undesended Testis in Children Hospital Faisalabad.
- ClinicalTrials.gov ID
- NCT07233265
- Acronym / sponsor ID
- CH-FSD -Orchidopexy- 2025
- Conditions
- Undescended Testis
- Keywords
- Orchidopexy, Scrotal incision, Inguinal incision, Paediatric surgery
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Children Hospital FaisalabadUniversity, hospital or other
- Study start
- Nov 2025 (estimated)
- Primary completion
- May 2026 (estimated)
- Study completion
- Jul 2026 (estimated)
- First posted
- 18 Nov 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study compares the outcome of single incision scrotal orchidopexy with standard two incision inguinal orchidopexy in children under 10 years of age presented with palpable undesended tesis.The aim is to evaluate operative time,cosmetic outcome and post operative complications.
Detailed description
All patients fulfilling the inclusion criteria admitted to paediatric surgery will be included by after taking informed consent from parents. Patients will be randomized in to two groups by lottery method.In group A ,orchidopexy is performed through single scrotal incision .In group B, orchidopexy is performed through standard two incision inguinal approach. This study compares the outcome interm of operative time, cosmetic outcome and post operative complications.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Single scrotal incision orchidopexy | Experimental | Procedure: Single scrotal incision orchidopexyChildren in this group undergoes single incision scrotal orchidopexy with palpable undesended testis in superficial inguinal canal. |
| Standard two incision inguinal orchidopexy | Active comparator | Procedure: Standard two incision inguinal orchidopexyChildren in this group undergoes standard two incision inguinal orchidopexy. |
Who may qualify
- Ages
- 12 months to 10 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Male children with age 1-10 years. Palpable low -lying undesended tesis.
Key exclusion criteria (1 listed)
- Impalpable testis Known bleeding disorder
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Single scrotal incision orchidopexyConventional orchidopexy performed through single scrotal incision | Procedure or surgery | Single scrotal incision orchidopexy |
| Standard two incision inguinal orchidopexyConventional orchidopexy performed through separate inguinal and scrotal incision | Procedure or surgery | Standard two incision inguinal orchidopexy |
Primary outcome
Post operative complications
Time frame: With in 24 hours -1month after surgery .
Numbers and type of post operative complications (Scrotal hematoma, infection, scrotal edema and testicular atrophy.
1 secondary outcome
Cosmetic outcome
Time frame: 2 weeks after surgery
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Nov 2025.
- Individual participant dataSharing planned: No
Related trials for Undescended Testis
Active, not recruitingObservational study
INVESTIGATION OF THE GENETIC ETIOLOGY OF HERNIA SAC DEVELOPMENT IN MALE CHILDREN WITH UNDESCENDED TESTIS AND INGUINAL HERNIA
Indirect Inguinal Hernia, Undescended Testis
Recruiting
Orchidopexy Randomized Clinical Assessment
Unilateral Cryptorchidism
Recruiting
Transection Versus Ligation of Internal Spermatic Vessels in Laparoscopic Fowler-Stephens Orchidopexy
Cryptorchidism
RecruitingObservational study
Role of the Environment and Endocrine Disruptors in Child Cryptorchidism
Cryptorchidism
Not yet recruiting
Learning to Palpate the Child's Testicles Using Simulation
Testicular Positioning Anomalies, Cryptorchidism
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Single scrotal incision orchidopexy and Standard two incision inguinal orchidopexy in people with Undescended Testis, run by Children Hospital Faisalabad at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 24 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Ijaz Ul Haq (03305611906, ijazulhaq1995@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Post operative complications (time frame: With in 24 hours -1month after surgery .). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Nov 2025.