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ASA Levels in TEP and Lichtenstein Repair Patients

A

Ankara City Hospital

Status

Unknown

Conditions

Hernia, Inguinal

Treatments

Procedure: TEP Repair
Procedure: Lichtenstein Repair

Study type

Interventional

Funder types

Other

Identifiers

NCT03355950
E-16-1019

Details and patient eligibility

About

The purpose of this study is to determine and compare the possible affects of two different inguinal hernia repair technique (TEP and Lichtenstein) on serum ASA levels.

Full description

Antisperm antibody levels are thought to be indirect indicators of spermatic duct injuries. The investigators' ultimate goal is to draw a conclusion about the effect of the type of surgery on spermatic duct integrity. The investigators are going to collect serum samples from inguinal hernia patients before and after surgery. The investigators aim to assess the effect of surgery on antisperm antibody levels of patients who undergo Licthenstein and TEP repair. Preoperative antisperm antibody levels will serve as control levels for each patient group.

Enrollment

160 estimated patients

Sex

Male

Ages

20 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • to accept the terms of the randomization and all study
  • to have unilateral inguinal hernia and set for an inguinal hernia repair
  • to be a father

Exclusion criteria

  • to have any kind of autoimmune disorders
  • any kind of infertility history
  • to have a history of inguinal and/or genital surgery and/or trauma

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

160 participants in 2 patient groups

TEP group
Active Comparator group
Description:
Patients who undergo totally extraperitoneal hernia repair, TEP Repair.
Treatment:
Procedure: TEP Repair
Lichtenstein group
Active Comparator group
Description:
Patients who undergo Lichtenstein repair.
Treatment:
Procedure: Lichtenstein Repair

Trial contacts and locations

1

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Central trial contact

Selami Ilgaz Kayılıoğlu, MD; Ömer Özduman, MD

Data sourced from clinicaltrials.gov

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