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High Intrabdominal Undescended TestisCOMPARISONNCT07421310

COMPARISON BETWEEN LAPAROSCOPIC TRACTION (SHEHATA TECHNIQUE) AND 2-STAGE FOWLER STEPHENS ORCHIOPEXY FOR HIGH INTRABDOMINAL UNDESCENDED TESTIS. A PROSPECTIVE RANDOMIZED STUDY.

A study testing Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy in people with High Intrabdominal Undescended Testis, run by Ain Shams University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this clinical trial is to compare between laparoscopic traction (Shehata technique) with 2-Stage Fowler Stephens orchiopexy in cases of high intra-abdominal undescended testis in a prospective randomized manner to verify the results of the Shehata technique against the reference standard Fowler-Stephens… Read more about this study

Who is it for?
Ages 6 months to 18 years, men only
Conditions the study is for
High Intrabdominal Undescended Testis
What is being tested?
Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteEgypt
Study dates
1 Jan 2024to 30 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

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 6 months to 18 years
  • Men only
  • No healthy volunteers
  • Child, Adult

Who may be able to join

  • Patients older than 6 months with impalpable undescended testis confirmed to be high intrabdominal testis after examination under anesthesia and laparoscopic exploration finding a testis that cannot be brought to scrotum in one stage as evidenced by failure to reach the contralateral internal inguinal ring.

Who cannot join

  • Patients who underwent previous abdominal surgery (intraperitoneal surgery).
  • Recurrent cases.
  • Patients older than 6 months with impalpable undescended testis with confirmed palpable testis after examination under anesthesia.
  • Patients older than 6 months with impalpable undescended testis with associated persistent Mullarian duct remnants.
  • Patients older than 6 months with impalpable undescended testis with confirmed intrabdominal testis which can be brought to scrotum in one stage after laparoscopic exploration. (Tensionless reach

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Department of Pediatric Surgery, Faculty of Medicine, Ain Shams University, Cairo, Egypt.

    Cairo, Cairo Governorate, 12345

Other trials in Egypt

About this study

The goal of this clinical trial is to compare between laparoscopic traction (Shehata technique) with 2-Stage Fowler Stephens orchiopexy in cases of high intra-abdominal undescended testis in a prospective randomized manner to verify the results of the Shehata technique against the reference standard Fowler-Stephens Orchiopexy in fullfilling the objective of placing a high intra-abdominal testis into the ipsilateral scrotal compartment without the occurance of later atrophy or ascent on follow up.

Type of Study: Prospective randomized clinical study that conforms to the CONSORT statement guidelines [9]. Patients will be divided into 2 groups randomized by block randomization method with an intention-to treat approach into:

Group 1: Patients will undergo the Shehata Traction technique. Group 2: Patients will undergo Folwer-Stephens technique.

Read the detailed description

Study Setting: The study will be conducted at the Department of Pediatric Surgery, Ain Shams University hospitals .

Study Period: 2 years from the approval from the Research Ethics Committee.

Study Population and CONSORT flowchart (Appendix 1)

  • Inclusion Criteria:
  1. Patients older than 6 months with impalpable undescended testis confirmed to be high intrabdominal testis after examination under anesthesia and laparoscopic exploration finding a testis that cannot be brought to scrotum in one stage as evidenced by failure to reach the contralateral internal inguinal ring.
  • Exclusion Criteria:
  1. Patients who underwent previous abdominal surgery (intraperitoneal surgery).
  2. Recurrent cases.
  3. Patients older than 6 months with impalpable undescended testis with confirmed palpable testis after examination under anesthesia.
  4. Patients older than 6 months with impalpable undescended testis with associated persistent Mullarian duct remnants.
  5. Patients older than 6 months with impalpable undescended testis with confirmed intrabdominal testis which can be brought to scrotum in one stage after laparoscopic exploration. (Tensionless reach

Sample Size Using a statistical sample power software (G*Power 3.1.9.7 for Windows, PsycInfo Database Record (c) 2022 APA) for sample size calculation, setting power at 90% and an α error at 5%, an estimated sample size of 44 children with Undescended testis (22 children undergoing laparoscopic traction of undescended testis "Shehata technique" \& 22 children undergoing Fowler Stephens orchiopexy) will be needed to detect a statistically significant difference between the two groups as regard overall success rate, assuming a large effect size difference (w"15) regarding Tian et al., 2023. At least 50 children with undescended testis(25 per group) will be needed. [10].

Sampling Method The patients will be assigned randomly using block randomization method with blocks of 4,6 allocation (Appendix 2). A web-based service is utilized for block generation (Sealed Envelope Ltd. 2022, Available from: https://www.sealedenvelope.com/simple-randomiser/v1/lists [Accessed 10 October 2023].

Ethical Considerations:

  1. The study will be presented for approval from the Research Ethical Committee (REC), Faculty of Medicine Ain shams University
  2. A detailed informed consent form (Appendix 3) will be discussed with the guardians highlighting the aim of the study, the merits of the procedure and expected complication nature \& rate as well as the plan of follow up.

Study Tools /Study Procedures/Study Interventions :

Laparoscopy will be used for either traction of the undescended testis or performing of Fowler- Stephens technique in a staged fashion.

  1. History taking The assessment of a child with undescended testis should begin with a history, considering risk factors such as prematurity and low birth weight and any co-morbidities.
  2. Examination: Local examination: After exhausting every effort to palpate the involved testis, the child is declared as having an impalpable undescended testis and booked for examination under anesthesia and proceed.
  3. Preoperative preparation: Routine preoperative investigation will be done.
  4. Operative details:

Commenced with examination under general anesthesia. If testis is impalpable at the inguinal region, a diagnostic laparoscopy follows:

  1. If the diagnostic laparoscopy reveals vanishing testis, the patient will be excluded from the study.
  2. If diagnostic laparoscopy reveals intrabdominal test is which can be brought to scrotum in one stage (as evidenced by ability of the testis to reach the contralateral internal ring with no/mild tension) the patient will be excluded from the study.
  3. Otherwise, a staged procedure traction technique or Fowler Stephens technique as per block allocation will be performed and this patient will be included in the study.

A: Two Stage Fowler-Stephen Technique

First Stage of Stephen Fowler Technique A 5 mm incision and port is placed in the left mid- epigastrium through with a 5 mm gasper forceps is introduced into the abdominal cavity. A 5 mm instrument is then placed in the right abdomen below the horizontal plane of umbilicus. Through this port a 5 mm endoclip applicator can be passed.

The peritoneum overlying the testicular vessels 2 cm cephalad to the testis is incised .The testicular vessels are then clipped or cauterized and divided.

When one is planning to perform orchidopexy in two stages, no dissection should be carried out in the vicinity of the testis in the first stage. The triangular leash of the peritoneum between the vas and vessels should not be dissected as it is here that a collateral circulation develops from the artery to the vas deferens and the peritoneal vessels.

Second Stage of Stephen Fowler Technique

In the second stage Stephen-Fowler procedure, again three ports are placed similar to the first stage. Now the testis is taken down on the leash of newly acquired collateral blood supply by inserting a 10 mm trocar through ipsilateral scrotum and the orchidopexy is completed.

B: Shehata Traction technique:

Preliminary traction to lengthen the testicular vessels by applying a 3/0 Ethibond suture to the testis fixing it to abdominal wall near the contralateral Anterior Superior Iliac Spine.

The second stage will be planned after 2 weeks similar in principle to the 2nd stage Fowler - Stephens orchiopexy.

During the first stage of either technique, the testis will be brought close to the anterior abdominal wall to enable a dedicated radiologist to perform an intraoperative ultrasound examination of the testis recording its dimensions as a baseline for further postoperative assessment.

  1. Follow up:

Early postoperative care:

Patients are operated on day-case basis and will be discharged on appropriate analgesics and instructions for follow up in the clinic/Radiology Department and booked for the second stage. Long term follow up:

Patients will be followed up by clinical examination conducted by an independent examiner and an Ultrasound study with Duplex verification of vascularity 3 months after discharge following the 2nd stage marking the end-point of the study.

Both the independent examiner and the radiologist will be blinded regarding technique used in each patient.

Success definition:

It defined by:

  1. Clinically palpable testis (non-atrophic), and
  2. Appropriate size compared to the initial intra-operative ultrasound examination of the testis (no more than 30% volume loss).
  3. Good vascularity proved by a Color Doppler 3 months after surgery.
  4. Testis residing in the bottom or middle of the scrotum (scrotal neck or inguinal testis are considered an ascent/failure).

Expected complications (Literature generated) :

  1. Atrophy/ smaller size(as a result of ischemic injury during dissection/clipping of the vessels).
  2. Ascending testis. (eligible for redo and inclusion as per intention-to treat principle)
  3. Slipped traction. (eligible for redo and inclusion as per intention-to treat principle)
  4. Severely Impaired vascularity (detected by Doppler)
  5. Intestinal adhesions or internal herniation.
  6. Injury to Vas Deferens.
  7. Epididymo-orchitis.
  8. Wound infection.
  9. Bleeding and hematoma.
Being tested
Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy
Keywords
Laparoscopic Traction (Shehata Technique), 2-Stage Fowler Stephens Orchiopexy, High Intrabdominal Undescended Testis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens OrchiopexyProcedure or surgery

    1. Operative details:

    Commenced with examination under general anesthesia. If testis is impalpable at the inguinal region, a diagnostic laparoscopy follows:

    1. If the diagnostic laparoscopy reveals vanishing testis, the patient will be excluded from the study.
    2. If diagnostic laparoscopy reveals intrabdominal test is which can be brought to scrotum in one stage (as evidenced by ability of the testis to reach the contralateral internal ring with no/mild tension) the patient will be excluded from the study.
    3. Otherwise, a staged procedure traction technique or Fowler Stephens technique as per block allocation will be performed and this patient will be included in the study.
Study groups in NCT07421310
Study groupRoleWhat they receive
Laparoscopic Traction (Shehata Technique)ExperimentalPreliminary traction to lengthen the testicular vessels by applying a 3/0 Ethibond suture to the testis fixing it to abdominal wall near the contralateral Anterior Superior Iliac Spine. The second stage will be planned after 2 weeks similar in principle to the 2nd stage Fowler - Stephens orchiopexy.
Receives: Procedure: Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy
2-Stage Fowler Stephens OrchiopexyExperimentalFirst Stage of Stephen Fowler Technique A 5 mm incision and port is placed in the left mid- epigastrium through with a 5 mm gasper forceps is introduced into the abdominal cavity. A 5 mm instrument is then placed in the right abdomen below the horizontal plane of umbilicus. Through this port a 5 mm endoclip applicator can be passed. The peritoneum overlying the testicular vessels 2 cm cephalad to the testis is incised .The testicular vessels are then clipped or cauterized and divided. When one is planning to perform orchidopexy in two stages, no dissection should be carried out in the vicinity of the testis in the first stage. The triangular leash of the peritoneum between the vas and vessels should not be dissected as it is here that a collateral circulation develops from the artery to the vas deferens and the peritoneal vessels. Second Stage of Stephen Fowler Technique In the second stage Stephen-Fowler procedure, again three ports are placed similar to the first stage. Now the
Receives: Procedure: Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Testicular Survival Rate and Successful Scrotal Position

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Feb 2026
  2. Study start1 Jan 2024
  3. Primary completion30 Nov 2025
  4. Study completion30 Nov 2025

Resources

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
Non-randomised
Intervention model
Parallel groups
Model description
Group 1: Patients will undergo the Shehata Traction technique. Group 2: Patients will undergo Folwer-Stephens technique.
Masking
None (open label)
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07421310
Sponsor's protocol ID
UNDESCENDED TESTIS
Other IDs
AinShamsU
Acronym
COMPARISON
Status last verified
Feb 2026
First submitted
12 Feb 2026
Last updated
19 Feb 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Laparoscopic Traction (Shehata Technique) And 2-Stage Fowler Stephens Orchiopexy in people with High Intrabdominal Undescended Testis, run by Ain Shams University at 1 site in Egypt.

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 5 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: finished, as of the sponsor's last update on 19 Feb 2026. 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 Egypt. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Testicular Survival Rate and Successful Scrotal Position (time frame: 2 years). 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 19 Feb 2026; AzTrials last refreshed its copy on 1 Nov 2026.

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