Skip to content

treatment of impalpable testis

Evaluation of effect of laparoscopic orchiopexy on descending testis in patients with non-palpable testis referred to surgery ward of Besat hospital of Hamedan and comparison with open surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103015945N1
Enrollment
50
Registered
2011-06-20
Start date
2009-05-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

impalpable testis. Undescended testicle, unilateral, Undescended testicle, bilateral, Undescended testicle, unspecified

Interventions

Intervention 1: Laparoscopy (minimally invasive procedure without requirement to surgical incision. Intervention 2: Open surgery in impalpable testis treatment.
Treatment - Surgery
Laparoscopy (minimally invasive procedure without requirement to surgical incision
Open surgery in impalpable testis treatment

Sponsors

Vice chancellor of research for Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
1 Years to 12 Years

Inclusion criteria

Inclusion criteria: inclusion criteria: aging range between 1 to 12 year's old ; patients with bilateral undescended testis without response to medical treatment with HCG Exclusion criteria: nonacceptance of patient's parents ; palpation of testis after anesthesia and before operation ; patient's death before ending of following time

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Testis existence in scrotum. Timepoint: 6 month. Method of measurement: palpation.

Secondary

MeasureTime frame
Scrotal hematoma. Timepoint: during 6 month after intervention. Method of measurement: observation and examination.;Surgical site infection. Timepoint: During 6 month after intervention. Method of measurement: Observation & examination.;Damage formation to gonadal vessels. Timepoint: During 6 month after intervention. Method of measurement: Observation & examination.;Injury to the vas deferens. Timepoint: During 6 month after intervention. Method of measurement: Observation & examination.;Mortality rate. Timepoint: During 6 month after intervention. Method of measurement: Observation & examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Majid Rezaii Tavirani

Hamedan University of Medical Sciences

tavirani.m@umsha.ac.ir+98 84 1223 9799

Outcome results

None listed

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