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Clinical Trials/NCT01665859
NCT01665859
Completed
Not Applicable

Nationwide Prospective Study of Surgical Risk Factors for Poor Outcome After Epigastric and Umbilical Hernia Repair

Zealand University Hospital1 site in 1 country6,783 target enrollmentJanuary 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Umbilical Hernia
Sponsor
Zealand University Hospital
Enrollment
6783
Locations
1
Primary Endpoint
readmission
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Umbilical and epigastric hernia repairs are common and performed by numerous surgical techniques. Considering that the hernia repairs in general are relatively small and simple procedures there are disproportionate poor results.

The aim of present study is to determine surgical risk factors for readmission after umbilical and epigastric hernia repair and to report risk factors for later reoperation for recurrence.

Detailed Description

All elective umbilical or epigastric hernias registered in the Danish Ventral Hernia Database are included in the study. The included patients will be followed in up to 4 years in order to identify correlation between technical aspects of the hernia repair and postoperative morbidity.

Registry
clinicaltrials.gov
Start Date
January 2007
End Date
July 2012
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Frederik Helgstrand

MD

Zealand University Hospital

Eligibility Criteria

Inclusion Criteria

  • Umbilical or epigastric hernia repair

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

readmission

Time Frame: 30 days

Riskfactors for readmission within 30 days after umbilical or epigastric hernia repair

Secondary Outcomes

  • reoperation for recurrence(up to 4 years)

Study Sites (1)

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