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Clinical Trials/NCT03326700
NCT03326700
Completed
Not Applicable

Effects of Laparoscopic Totally Extraperitoneal and Lichtenstein Hernia Repair on Men's Sexual Functions and Quality of Life.

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization0 sites176 target enrollmentNovember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hernia, Inguinal
Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Enrollment
176
Primary Endpoint
IIEF Scale
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

In the literature, there are several studies that compare Laparoscopic totally extraperitoneal hernia repair (TEP) with Lichtenstein hernia (LH) repair. There are no studies that compare sexual functions on men's health and quality of life. Our aim was to study the sexual functions of men, who underwent TEP or LH repair according to Health Survey Scoring Demonstration (SF36) and The International Index of Erectile Function (IIEF).

Detailed Description

176 men with unilateral inguinal hernia were randomized into two groups. Group T (n=88) underwent TEP and Group L(n:88) underwent LH repair. Patients demografigs, perioperative findings were recorded. For all patients preoperative, postoperative 7th,30th and 90th day SF 36 and IIEF were filled up.

Registry
clinicaltrials.gov
Start Date
November 2015
End Date
May 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization
Responsible Party
Principal Investigator
Principal Investigator

Riza Gurhan ISIL

MD

Prof. Dr. Cemil Tascıoglu Education and Research Hospital Organization

Eligibility Criteria

Inclusion Criteria

  • having male gender
  • patients diagnosed on unilateral inguinal hernia
  • patients aged between 18 and 65 years
  • ASA I and II patients

Exclusion Criteria

  • having female gender
  • patients diagnosed on bilateral or recurrence inguinal hernia,
  • patients suffering erectile dysfunction

Outcomes

Primary Outcomes

IIEF Scale

Time Frame: 7 to 90 days

international index of erectile functions

Secondary Outcomes

  • SF36(7 to 90 days)

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