Observation study using titanized mesh for inguinal hernia repair

Phase 4

• Conditions: K40; Inguinal hernia

• Registration Number: DRKS00021043
• Lead Sponsor: St. Bernhard-Hospital GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-11-04
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

inguinal hernia (EHS 1 and 2)

Exclusion Criteria

inguinal hernia EHS 3, NOAK until surgery, cumarine until surgery, plavix until surgery, immunosupressive medication, hernia recurrence, hernia on both sides

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hernia recurrence: follow-up 1 year

Secondary Outcome Measures

Name	Time	Method
Pain, wound infection, foreign body Sensation:<br>follow-up 1 Year