Risk Factors and Results of Emergency Ventral Hernia Repair

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT01589276

Enrollment

10976

Registered

2012-05-01

Start date

2007-01-31

Completion date

2012-02-29

Last updated

2018-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ventral Hernia

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

Interventions

None listed

Study design

Observational model

CASE_CONTROL

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* All incisional, umblilical and epigastric hernia repiars

Design outcomes

Primary

Measure	Time frame	Description
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

Measure	Time frame	Description
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
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

Countries

Denmark

Outcome results