Late Mesh Complications After 3258 Incisional Hernia Operations

NCT ID: NCT02263612

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

3258 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-31

Study Completion Date

2015-09-30

Brief Summary

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The Danish Hernia Database (DHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DHD to uncover risk factors for long-term (30 days postoperative and later) readmission, reoperation, death and reoperation for recurrence after incisional hernia repair with use of a synthetic mesh.

Detailed Description

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All principal incisional hernias registered in the Danish Hernia Database are included in the study. The included patients have been followed for more than 4 years in order to identify correlation between technical aspects of the hernia repair and postoperative morbidity.

Conditions

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Incisional Hernia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Danish Hernia Database

Patients registered in the Danish Ventral Hernia Database during January 1st 2007 to december 31st 2010

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Incisional Hernia Repair
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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Dunja Kokotovic, MS

Role: PRINCIPAL_INVESTIGATOR

dept. of surgery, Køge University Hospital

Locations

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Køge Sygehus

Køge, , Denmark

Site Status

Countries

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Denmark

Other Identifiers

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DK_02

Identifier Type: -

Identifier Source: org_study_id

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