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OpenTrials
Completed

NCT Number: NCT01589276

Risk Factors and Results of Emergency Ventral Hernia Repair

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.

Completed

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Key information

Conditions

Ventral Hernia Hernia Hernia, Abdominal Hernia, Ventral Pathological Conditions, Anatomical Pathological Conditions, Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Dept. of Surgery, Køge Hospital

Køge, 4600, Denmark

About this study

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

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All incisional, umblilical and epigastric hernia repiars

Treatment and study plan

Primary outcomes

  1. risk factors for emergency ventral hernia repair

    Time frame: 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 outcomes

  1. 30-day readmission

    Time frame: 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

  2. 30-day reoperation

    Time frame: 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

  3. 30-day mortality

    Time frame: 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

Sponsors and collaborators

Lead sponsor

Zealand University Hospital

Other

Registry information

Important dates

Study start
2007
Primary completion
2011
Study completion
2012
First posted
May 1, 2012
Registry last updated
Jun 27, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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