Risk Factors and Results of Emergency Ventral Hernia Repair

NCT ID: NCT01589276

Last Updated: 2018-06-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

10976 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-31

Study Completion Date

2012-02-29

Brief Summary

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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

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

Conditions

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Ventral Hernia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Emergency hernia repairs

No interventions assigned to this group

Elective hernia repairs

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* All incisional, umblilical and epigastric hernia repiars
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Zealand University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Frederik Helgstrand

MD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Frederik Helgstrand, MD

Role: PRINCIPAL_INVESTIGATOR

dept. surgery, Køge sygehus, Denmark

Locations

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Dept. of Surgery, Køge Hospital

Køge, , Denmark

Site Status

Countries

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Denmark

References

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Helgstrand F, Rosenberg J, Kehlet H, Bisgaard T. Outcomes after emergency versus elective ventral hernia repair: a prospective nationwide study. World J Surg. 2013 Oct;37(10):2273-9. doi: 10.1007/s00268-013-2123-5.

Reference Type DERIVED
PMID: 23756775 (View on PubMed)

Other Identifiers

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FH08

Identifier Type: -

Identifier Source: org_study_id

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