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One stage laparoscopic abdominal testis orchiopexy in supine position Vs novel method of laparoscopic orchiopexy in lateral decubitus position with colon medialization

Evaluation of the efficacy of one stage laparoscopic abdominal testis orchiopexy in supine position vs novel method of laparoscopic orchiopexy in lateral decubitus position with colon medialization as a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200905048625N2
Enrollment
52
Registered
2022-05-09
Start date
2022-06-10
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Abdominal testis orchiopexy. Abdominal testis, unilateral

Interventions

Intervention 1: Intervention group: one stage laparoscopic abdominal testis orchiopexy in supine position. Intervention 2: Intervention group: novel method of laparoscopic orchiopexy in lateral decubi

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
12 Months to 15 Years

Inclusion criteria

Inclusion criteria: Untouchable testicles, Which is available in laparoscopy and requires archiopexy. Consent to participate in the study Peeping testis,The testicles are pressed only on the abdomen and in the upper part of the inguinal canal

Exclusion criteria

Exclusion criteria: Patients with palpable testicles in the middle of the canal, and scrotum Blind end vessel and vanished testi Patients over 15 years old Redo patients Patients splenic fusion or other rare types of abnormalities associated with testicular prolapse (such as Persistent Müllerian Duct Syndrome) Differences in sex development

Design outcomes

Primary

MeasureTime frame
The rate of testicular descent. Timepoint: 10 days, 6 weeks and six months after surgery. Method of measurement: Examination of the patient by a physician.

Secondary

MeasureTime frame
The rate of complete atrophy at the time of follow-up. Timepoint: 10 days, 6 weeks and six months after surgery. Method of measurement: Examination of the patient by a physician.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Akram Mirzaei

Tehran University of Medical Sciences

mirzaee.scholar@gmail.com+98 21 6634 8560

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026