A Comparative Study of results of Ligation hernia Surgery SAC in Orchiopexy Childrens with Undescended Testis

A Comparative Study of Surgery results with and without Ligation hernia SAC in Orchiopexy Childrens with Undescended Testis

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2015101214333N42

Enrollment

Registered

2015-10-27

Start date

2013-09-06

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

Undescended testicle, bilateral. Undescended testicle, bilateral

Interventions

Intervention 1: The hernia sac ligation surgery was performed in the experimental group, Then the hematoma and bleeding, hydrocele, wound infection, recurrence, swelling and cord inflammation was reco

Treatment - Surgery

The hernia sac ligation surgery was performed in the experimental group, Then the hematoma and bleeding, hydrocele, wound infection, recurrence, swelling and cord inflammation was recorded and patient

The hernia sac ligation surgery was not performed in the control group, Then the hematoma and bleeding, hydrocele, wound infection, recurrence, swelling and cord inflammation was recorded and patients

Eligibility

Sex/Gender

Male

Age

1 Years to 10 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: children 1 to 10 years old with undescended testis;written consent of the patient or the patient's guardian. Exclusion criteria: clinical inguinal hernia (visible) along with undescended testis;hernia stuck with undescended testis; deterrent hernia along with undescended testis; increased intra-abdominal pressure for any reason (dialysis, etc.) along with undescended testis.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Hematoma and bleeding. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the surgeon examination.;Wound infection. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: Based on the clinical symptoms and physician observation.;Swelling and cord inflammation. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the sonography and physician observation.;Recurrence after operation. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the sonography and physician observation.	—

Measure

Time frame

Hematoma and bleeding. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the surgeon examination.;Wound infection. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: Based on the clinical symptoms and physician observation.;Swelling and cord inflammation. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the sonography and physician observation.;Recurrence after operation. Timepoint: A week after the operation and one, three and six months after the operation. Method of measurement: According to the sonography and physician observation.

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Countries

Iran (Islamic Republic of)

Outcome results

None listed

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