Comparison of different durations of physical activity restrictions following incisional hernia repair in sublay technique, the 3N6 Trial: A prospective clinical trial

Not Applicable

• Conditions: K43.9; Other and unspecified ventral hernia without obstruction or gangrene

• Registration Number: DRKS00021020
• Lead Sponsor: HELIOS Klinikum Berlin-Buch

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-05-12
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Over the age of 18, consent to the participation in the study, and have an incisional hernia > 2cm.

Exclusion Criteria

Occurrence of postoperative complications such as wound infection, DVT, and secondary interventions, pregnancy, a non-treated HIV infection, residence >200km from the hospital.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary endpoint is the duration of sick leave that patients require either to return to work or to resume their normal daily activities, by comparing PAR of 6 weeks with PAR of 3 weeks.

Secondary Outcome Measures

Name	Time	Method
The secondary endpoint is the one-year recurrence rate.