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

• Conditions: ARBENHERNIA; K43.0; Incisional hernia with obstruction, without gangrene

• Registration Number: DRKS00020974
• Lead Sponsor: Helios Klinikum Berlin-Buch

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-07-06
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting withdrawn before recruiting started
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

Patients, who underwent incisional hernia repair.

Exclusion Criteria

Patients, who did not underwent incisional hernia repair.

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time of reoperation (years)

Secondary Outcome Measures

Name	Time	Method
Rate of seroma, relapses on 365. POD, Clavien-Dindo-classification within 30 days after surgery