Pain after Kugel versus Lichtenstein repair: a randomized trial.

Completed

• Registration Number: NL-OMON22718
• Lead Sponsor: /A

Brief Summary

World J Surg. 2007 Sep;31(9):1751-7; discussion 1758-9. Epub 2007 May 18.

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 172

Inclusion Criteria

Adult patients who had been referred for elective primary, unilateral inguinal hernia repair and gave informed consent.

Exclusion Criteria

An irreducible inguinoscrotal hernia or previous procedures using the preperitoneal approach.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
VAS pain score at three months postoperatively.

Secondary Outcome Measures

Name	Time	Method
VAS pain scores and consumed analgesics during the first two weeks postoperatively, Pain Disability Index scores, neuroligical disturbances.