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Clinical Trials/NCT06257459
NCT06257459RecruitingNot Applicable

Excision Versus Preservation of Spermatic Cord Lipoma Detected During Subinguinal Varicocelectomy in Infertile Men With Oligo-asthenzoospermia: A Prospective Randomized Trial.

Tanta University2 sites in 1 country200 target enrollmentStarted: January 1, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
200
Locations
2
Primary Endpoint
semen parameters improvement

Study Overview

Brief Summary

In the current study, the adult infertile patients with clinical varicoceles will be included. the patients will undergo subinguinal varicocelectomy. The patients with spermatic cord lipoma detected at the time of surgery will be enrolled and divided into 2 groups( excision group, group A and preservation group (B). semen parameters will be compared in both group at 3 and 6 months after surgery

Detailed Description

This will be a prospective randomized study, in which adult infertile patients with clinical varicocele and oligo-athenospermia admitted to Urology department Tanta university hospital will be included and then the patients with detected spermatic cord lipoma at the time surgery will be enrolled and divided into 2 groups:

GROUP A : will undergo subinguinal varicocelectomy with excision of spermatic cord lipoma GROUP B : will undergo subinguinal varicocelectomy with preservation of spermatic cord lipoma

Inclusion criteria:

  • Adult infertile males
  • Clinical varicocele
  • oligo-asthenospermia

Exclusion criteria:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adult infertile males
  • Clinical varicocele
  • Semen analysis show oligo-athenospermia

Exclusion Criteria

  • Adolescent varicocele
  • Recurrent varicocele
  • Presence of inguinal hernia
  • Azospermic patients

Outcomes

Primary Outcomes

semen parameters improvement

Time Frame: 3 and 6 months after surgery

semen analysis

symptoms improvement (pain and swelling)

Time Frame: 3 and 6 months after surgery

improvement of preoperative scrotal pain and swelling was assessed

Secondary Outcomes

  • postoperative complications(early after surgery and late)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Zoeir

faculty of medicine, Tanta, ElGeish street, Egypt

Tanta University

Study Sites (2)

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