Shehata Technique in the Treatment of Intra-abdominal Testis

BACKGROUND AND STUDY AIMS Cryptorchidism, defined as the absence of one or both testicles from the scrotum, is the most common congenital genital anomaly identified at birth. The standard surgical treatment-orchiopexy-involves repositioning the testicle within the scrotal sac. Approximately 30% of cases involve "non-palpable testicles," which necessitate diagnostic laparoscopy as the preferred method for both diagnosis and treatment. A procedure is considered effective and safe when the testicle is successfully relocated to the scrotum without atrophy.

The most challenging form of cryptorchidism occurs when testicles are intra-abdominal with short testicular vessels, precluding primary descent. In these cases, the Fowler-Stephens technique has been developed; it involves dividing the testicular vessels to permit descent during a second surgical stage. However, this method is not without complications, with testicular atrophy being one of the most common adverse outcomes.

To address these issues, the Shehata technique was introduced in 2008, demonstrating a 100% success and safety rate in achieving scrotal descent without testicular atrophy. This impressive outcome relies on an intraoperative maneuver that assesses the vascular pedicle length, thereby guiding the choice of procedure (VILO vs. Shehata). Nonetheless, there is currently insufficient evidence to fully validate the significance of this maneuver. Therefore, the objectives of this study are to evaluate the safety and efficacy of the Shehata and VILO laparoscopic techniques for the descent of intra-abdominal testicles.

Who can participate? All patients from 6 months to 7 years of age, with intra-abdominal cryptorchidism confirmed by laparoscopy, non-syndromic, unilateral or bilateral What does the study involve? Patients will undergo a laparoscopic descent with preservation of testicular vessels, either a primary descent (VILO) or by means of the elongation and delayed descent technique (Shehata). Six months after surgery, testicular atrophy (safety) and intrascrotal placement (efficacy) will be determined by ultrasound and clinical examination, with the same subject being monitored before and after the intervention.

Where is the study run from? Instituto Nacional de Pediatría (México) When is the study starting and how long is it expected to run for? February 2025 to December 2025 Who is funding the study? Instituto Nacional de Pediatría (México) Who is the main contact? Silvio Carmona. Silviodocmor@hotmail.com STUDY DESIGN Study design: Quasi-experimental study Primary study design: Interventional Secondary study design: Quasi-Experimental Approach Study setting(s): Hospital Study type: Safety, Efficacy

Participant information sheet Study hypothesis

• The VILO technique will be effective and safe, with a success rate of over 90% and less than 5% testicular atrophy.
• The Shehata technique will be effective and safe, with a success rate of over 90% and less than 5% testicular atrophy.

Ethics approval(s) Approved: Dec 10 dic 2025, by Research Committee and Research Ethics Committee of the Instituto Nacional de Pediatria Number of Registry: 2024/063

Condition: Intrascrotal relocation of the intra-abdominal testicles is essential to improve the future fertility of patients,.

Intervention: Patients will be recruited from the surgical outpatient clinic with a diagnosis of cryptorchidism involving a non-palpable testicle. After a medical evaluation by an attending physician confirming the clinical presentation of a "non-palpable testicle," these patients will be invited to participate in the study. The parents of the participants will be informed about the patient's diagnosis, the available diagnostic and therapeutic options, and the necessary follow-up. The study protocol will include: a complete blood count, coagulation times, and a preoperative inguino-scrotal ultrasound .

The intraoperative measurement of the vascular pedicle length will determine whether the VILO or Shehata technique is employed.

VILO Group:

For patients whose intra-abdominal testicle reaches the contralateral internal inguinal ring without difficulty-and when, with the aid of a second laparoscopic clamp, the vascular pedicle and vas deferens can be elevated to contact the anterior abdominal wall , a primary descent will be performed.

Shehata Group:

For testicles that, despite gentle and extensive mobilization, require an attempt to lift the mesentery until it contacts the abdominal wall, if the resulting length is insufficient, a staged laparoscopic orchiopexy preserving the testicular vessel described by will be performed. This procedure involves contralateral fixation of the intra-abdominal testicle above the contralateral iliac crest using a vascular prolene suture, thereby preserving the testicular vessels as well as the vas deferens and its circulation. The procedure is then concluded with the closure of the laparoscopic incisions, and the patient is transferred to recovery.

Subsequently, a follow-up is scheduled at 12 weeks, preceded by an abdominal Doppler ultrasound to document the testicle's position and characteristics before the second surgical stage. During this second laparoscopic stage, once the testicle is located, it is freed from its fixation to the abdominal wall, and the final elongation of the vascular pedicle is documented using the same maneuver described by Shehata . The testicle is then descended through an ipsilateral paravesical neotract until it is externalized via an incision in the mid-third of the scrotum, where it is secured with two prolene sutures to the scrotal dartos.

Follow-Up Protocol:

• First Consultation (7-10 days postoperatively): Assessment of the healing of the laparoscopic incisions and, for those who underwent scrotal orchiopexy, the scrotal incision.

• Second Consultation (12-13 weeks postoperatively): Evaluation of the preliminary clinical outcomes regarding testicular position, and exclusion of postoperative complications such as inguinal hernia, umbilical hernia, and testicular atrophy. An inguino-scrotal ultrasound will also be performed to determine gonadal size and to re-measure both inguinal orifices.

• Third Consultation (6 months postoperatively): Clinical review, including a Doppler ultrasound evaluation to measure testicular volume, dimensions, and to assess for any abdominal wall defects.

• Fourth Consultation (12 months postoperatively): Clinical review, including a Doppler ultrasound evaluation to measure testicular volume, dimensions, and to assess for any abdominal wall defects.

• Annual Follow-Up: Color Doppler ultrasound examinations with testicular measurements and clinical evaluations.

Primary outcome measure Efficacy will be considered achieved if the corrected testicle remains in the lower or middle portion of the scrotum.

Safety will be determined by the preservation of more than 75% of the initial volume as calculated by ultrasound, maintenance of normal vascularity, or as assessed by direct measurements at the time of descent into the scrotum.

Secondary outcome measures Testicles that are positioned in the high or upper scrotum, those with a reduction in testicular volume to less than 75% of the original, or those with abnormalities on color Doppler will be considered as failed corrections.

The overall study start date is 01/01/2025 The overall study end date is 06/01/2027

Eligibility Participant type(s) Patient Age group 6 meses a 7 años de edad Sex Both Target number of participants 30 Participant inclusion criteria

• Patients with non-syndromic intra-abdominal cryptorchidism confirmed by laparoscopy.
• Patients whose parents or guardians sign an informed consent form for their inclusion.
• Patients from Mexico City or areas close to the city who can attend follow-up Participant exclusion criteria
• Patients with other concomitant genital abnormalities (e.g. hypospadias) Recruitment start date 02/25/2025 Recruitment end date 01/01/2026