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CompletedNCT07353164Updated Jan 20, 2026

Comparison of Open Versus Laparoscopic High Ligation Varicocelectomy For The Treatment Of Varicocele

An interventional study of Open high ligation varicocelectomy and Laparoscopic high ligation varicocelectomy in Varicocele, sponsored by Lahore General Hospital. Completed at 1 site in Pakistan. Open to male participants aged 20 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-01-20.

Sponsored by Lahore General Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 4 months after the study started (first participant enrolled Sep 2024, registered Jan 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
20 Years to 60 Years
Sex
Male
01

Study summary

Varicocele is a common condition in which veins around the testis become enlarged, and it may be associated with scrotal discomfort and reduced fertility. Surgical treatment aims to stop the backward flow of blood in these veins so that the testicular environment improves. This randomized controlled trial was conducted in the Department of Urology, PGMI, Lahore General Hospital, Lahore, over a six-month period.

Male patients aged 20 to 60 years with diagnosed varicocele and planned varicocelectomy under general anesthesia were enrolled after informed consent. Patients with recurrent varicocele, secondary varicocele, associated undescended testis, or a history of orchidopexy were excluded. Eligible participants were allocated into two groups using a lottery method. In Group A, high ligation was performed by the open method through a lower abdominal incision, with identification and ligation of the dilated testicular veins at a high level. In Group B, high ligation was performed laparoscopically using three small ports, with the testicular vein identified, clipped, and divided. Standard perioperative care was provided, including intravenous antibiotics and postoperative analgesia.

The study compared the two techniques in terms of mean operation time , length of hospital stay , and wound infection . The hypothesis was that a difference existed between open and laparoscopic high ligation varicocelectomy regarding operation time, hospital stay, and wound infection.

02

Conditions studied

  • Varicocele

Keywords

  • Varicocelectomy
  • High ligation
  • Open surgery
  • Laparoscopic surgery
  • Postoperative wound infection
03

In context

Varicocele

53 studies on the registry are indexed under Varicocele; 15 are open to participants now.

This study's enrollment of 100 is above the median of 72 across 36 interventional studies indexed under Varicocele.

Browse Varicocele studies →

Lead sponsor

Lahore General Hospital is the lead sponsor of 32 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 60 Years
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male patients age 20-60 years.
  • Patients with varicocele.
  • Planned to undergo varicocelectomy under general anesthesia.

Exclusion criteria

Exclusion Criteria:

  • Patients with recurrent varicocele.
  • Secondary varicocele.
  • Associated undescended testis or history of orchidopexy.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
100 participants (actual)

Study arms

  • Experimental
    Group A (Open high ligation varicocelectomy)

    Open high ligation varicocelectomy

    Procedure: Open high ligation varicocelectomy

  • Active comparator
    Group B (Laparoscopic high ligation varicocelectomy)

    Laparoscopic high ligation varicocelectomy

    Procedure: Laparoscopic high ligation varicocelectomy

Interventions

  • ProcedureOpen high ligation varicocelectomy

    High ligation of the dilated testicular veins was performed by an open approach through a lower abdominal incision. The spermatic cord structures were approached extraperitoneally, the testicular vein was identified, separated from the artery after identification, and divided with ligatures. Wound closure was performed in layers with absorbable sutures and skin closure with silk sutures.

  • ProcedureLaparoscopic high ligation varicocelectomy

    High ligation of the testicular vein was performed laparoscopically by inserting three ports. The testicular vessels were approached intraperitoneally, the testicular vein was identified, clipped, and divided. Wound closure was performed using absorbable suture material, with skin closure using silk sutures.

06

What researchers measure

Primary outcomes

  1. Mean operative time

    Operative time was measured in minutes from skin incision until completion of skin closure (stitching).

    Time frame: During the surgery

Secondary outcomes

  1. Length of hospital stay

    Hospital stay was measured in days from the day of surgery until discharge from the hospital.

    Time frame: Up to 30 days post-surgery

  2. Wound infection rate

    Wound infection was assessed at 10 days after surgery with confirmation by positive pus culture when discharge was present.

    Time frame: 10 days after surgery

07

Study locations

1 site
  • Lahore General Hospital, Lahore
    Lahore, Punjab Province 54000, Pakistan
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07353164
Lead sponsor
Lahore General Hospital
Responsible party
Muhammad Irfan Jamil (Principal Investigator, Lahore General Hospital) — Principal investigator
First posted
Jan 20, 2026
Start date
Sep 1, 2024
Primary completion
Nov 30, 2025
Completion
Nov 30, 2025
Last update
Jan 20, 2026

Study contacts

Muhammad Zeshan Aziz
principal investigator · Lahore General Hospital, Lahore

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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