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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01484743
Other study ID # Parastoma
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2007
Est. completion date October 2011

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 Danish Ventral Hernia Database (DVHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DVHD to uncover risk factors for readmission, reoperation (any indication), death and reoperation for recurrence after parastomal hernia repair.


Description:

All principal parastomal hernias registered in the Danish Ventral Hernia Database are included in the study. The included patients will be followed in up to 4 years in order to identify correlation between technical aspects of the hernia repair and postoperative morbidity.


Recruitment information / eligibility

Status Completed
Enrollment 199
Est. completion date October 2011
Est. primary completion date December 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All parastomal hernia repairs registered in the Danish National Ventral Hernia Database

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
differences in surgical techniques
follow the risk for morbidity after incisional hernia repair

Locations

Country Name City State
Denmark Køge Hospital Køge Region Sjælland

Sponsors (1)

Lead Sponsor Collaborator
Zealand University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recurrence repair Surgical risk factors for recurrence repair after parastomal hernia repair. up to 4 years after operation
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