Risk Factors and Results of Emergency Ventral Hernia Repair

Completed

• Conditions: Ventral Hernia

• Registration Number: NCT01589276
• Lead Sponsor: Zealand University Hospital

Brief Summary

The aim of present study was to evaluate the clinical course after emergency ventral hernia repair in terms of 30-day-readmission, -reoperation and -mortality and to identify risk factors for emergency repair.

Detailed Description

All incisional, umbilical and epigastric hernias registered in the Danish Ventral Hernia Database

Study Timeline

• Study Start: 2007-01
• Primary Completion: 2011-01
• Study Completion: 2012-02
• Study First Submitted: 2012-04-26
• Study First Submitted QC: 2012-04-28
• Study First Posted: 2012-05-01
• Status Verified: 2018-06
• Last Update Submitted: 2018-06-26
• Last Update Posted: 2018-06-27

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10976

Inclusion Criteria

• All incisional, umblilical and epigastric hernia repiars

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
risk factors for emergency ventral hernia repair	4 years	evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for poor outcome after emergency ventral hernia repair.

Secondary Outcome Measures

Name	Time	Method
30-day reoperation	30 day	evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for 30-day reaoperation after emergency ventral hernia repair
30-day mortality	30 day	evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for 30-day mortality after emergency ventral hernia repair
30-day readmission	30 days	evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for 30-day readmission after emergency ventral hernia repair

Trial Locations

Locations (1)

Dept. of Surgery, Køge Hospital; 🇩🇰 Køge, Denmark