sefulness of the abdominal binder as postoperative treatment following incisional hernia repair

Not Applicable

• Conditions: K43.98; K40.91; K43; R52; Ventral hernia; Pain, not elsewhere classified

• Registration Number: DRKS00015665
• Lead Sponsor: Helios Forschungsförderung der Helios Kliniken

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2019-05-16
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients who have an incisional hernia
Surgical treatment using laparoscopic IPOM technology
Cognitive ability to give informed consent

Exclusion Criteria

Known HIV infection
Refusal to participate in the study on the part of the patient
Pregnancy

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain after 1.,2. and 14. postoperative day following incisional hernia repair in IPOM technique

Secondary Outcome Measures

Name	Time	Method
Seromas, wound infection, relapse on 1st, 2nd and 14th<br>postoperative day<br><br>Restriction of mobility according to VAS on the 1st, 2nd and 14th postoperative day<br><br>General well-being according to VAS on the 1st, 2nd and 14th<br>postoperative day<br><br>Postoperative complications according to the Clavien-Dindo classification and compliance with (NOT) bandaging on the 14th postoperative day<br><br>Quality of life after one year according to SF36 questionnaire<br>One year recurrence rate