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Single Incision Laparoscopic Varicocelectomy

Single Incision Transumbilical Laparoscopic Varicocelectomy: Comparison With the Conventional Laparoscopic Approach.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02335385
Enrollment
90
Registered
2015-01-09
Start date
2009-06-30
Completion date
2012-06-30
Last updated
2015-01-09

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

Conditions

Varicocele

Brief summary

Conventional laparoscopic varicocelectomy using 3 ports has been used for treatment of varicocele in our department since the nineties. However, the relatively several trocar wounds represent a big challenge against its acceptance by many of our patients who prefer the open approach with one or at least two wounds. Single incision laparoscopic surgery (SILS), since its introduction in 2007, has been proven to be feasible and effective, with high patient satisfaction rates regarding improved cosmotic outcomes, reduced postoperative pain, and rapid return to normal activities. (10, 11) SILS for varicocelectomy has been reported to be safe and effective alternative to conventional laparoscopic varicocelectomy in a few studies.

Interventions

PROCEDUREsingle incision laparoscopic varicocelectomy

bilateral and unilateral varicocelectomy was performed through a single transumbilical flexible SILS port.

PROCEDUREconventional transperitoneal laparoscopic varicocelectomy

bilateral and unilateral varicocelectomy was performed through a conventional 3-ports transperitoneal varicoceletomy

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients with palpable varicoceles

Exclusion criteria

* unfit for anesthesia or laparoscopy

Design outcomes

Primary

MeasureTime frame
number of patients with improvement in semen parameters and resolution of testicular pain2 years

Secondary

MeasureTime frame
number of patients developing postoperative complications2 years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026