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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01501682
Other study ID # ventralexmesh_KoegeHospital
Secondary ID
Status Recruiting
Phase N/A
First received December 18, 2011
Last updated December 28, 2011
Start date February 2011
Est. completion date December 2011

Study information

Verified date December 2011
Source Koege Sygehus
Contact Frederik helgstrand, MD
Email freh@regionsjaelland.dk
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to compare the long-term complaints after ventral hernia repair after insertion of different types of mesh compared with primary suture. Also recurrence of hernia will be discussed.


Description:

The purpose of this study is to compare the long-term complaints after ventral hernia repair after insertion of different types of mesh compared with primary suture. Based on a questionnaire selected patients will be invited to clinical examination for recurrence and more detailed interview.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- operated for ventral hernia from the year 2004 to the year 2009

Exclusion Criteria:

- liver cirrhosis

- pregnancy

- combined hernia

- operation for ventral hernia and other operation

- laparoscopic operation

- acute operation

- recurrence of hernia

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Koege hospital Koege
Denmark Køge sygehus Køge

Sponsors (1)

Lead Sponsor Collaborator
Koege Sygehus

Country where clinical trial is conducted

Denmark, 

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