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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02292264
Other study ID # HS_01
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 2014
Est. completion date June 2015

Study information

Verified date June 2018
Source Zealand University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study is to evaluate risk factors and complications of ventral hernia repair. A retrospective study of journal files with patients undergoing ventral hernia repair, and an analyses of complications by use of the Clavien-Dindo classification of surgical complications.


Recruitment information / eligibility

Status Completed
Enrollment 575
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Surgically treated ventral hernia repair

Exclusion Criteria:

- All surgically treated patients are included

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Køge University Hospital Køge

Sponsors (1)

Lead Sponsor Collaborator
Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identifying pre-operative risk factors by use of the Clavien Dindo classification. 5 years
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