The treatment of recurrent inguinal hernias after posterior repair

Recruiting

• Conditions: groin hernia; inguinal hernia; 10010761; 10041297

• Registration Number: NL-OMON34618
• Lead Sponsor: Slotervaartziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

patients who had laparoscopic recurrent inguinal hernia repair, after previous posterior repair

Exclusion Criteria

none

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Outcomes<br /><br>To evaluate the safety of a laparoscopic correction of a recurrent hernia after<br /><br>previous posterior hernia repair, the following outcomes will be assessed:<br /><br>• Complications during surgery, such as collateral damage or conversion<br /><br>• Complications after surgery, such as wound infection, hematoma or seroma<br /><br>• Pain or discomfort in the groin and possible restrictions in daily activities<br /><br>• Presence of a recurrence<br /><br>• Presence of a port site hernia<br /><br>• Days of admission</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>none</p><br>