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NCT01589276 Clinical Trial

Risk Factors and Results of Emergency Ventral Hernia Repair

Ventral Hernia Clinical Trial

Official title:
Risk Factors and Results of Emergency Ventral Hernia Repair

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01589276
Other study ID # FH08
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2007
Est. completion date February 2012

Study information
Verified date June 2018
Source Zealand University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

Description:

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

Recruitment information / eligibility
Status Completed
Enrollment 10976
Est. completion date February 2012
Est. primary completion date January 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All incisional, umblilical and epigastric hernia repiars

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Dept. of Surgery, Køge Hospital Køge

Sponsors (1)
Lead Sponsor Collaborator
Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome
Type Measure Description Time frame Safety issue
Primary risk factors for emergency ventral hernia repair evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for poor outcome after emergency ventral hernia repair. 4 years
Secondary 30-day readmission evaluation of risk factors (hernia size, hernia type, type of surgery, age and gender) for 30-day readmission after emergency ventral hernia repair 30 days
Secondary 30-day reoperation 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
Secondary 30-day mortality 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
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