Status:
UNKNOWN
Intraperitoneal Mesh-Implementation After Laparotomy
Lead Sponsor:
Kantonsspital Liestal
Conditions:
Incisional Hernia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Aim of the study is to evaluate the risk reduction of intraperitoneal mesh-implementation after laparotomy (Group 1) in a randomized control trial compared with patients with standard abdominal closur...
Eligibility Criteria
Inclusion
- Informed consent
- Median Laparotomy
Exclusion
- Bowel perforation
- Pregnancy
- Palliative surgery
- Drug abuse
- Age under 18
- Mental disability
- Allergy to mesh components
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
June 1 2020
Estimated Enrollment :
267 Patients enrolled
Trial Details
Trial ID
NCT01003067
Start Date
March 1 2008
End Date
June 1 2020
Last Update
August 15 2019
Active Locations (1)
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1
Kantonsspital Liestal
Liestal, Basel-Landschaft, Switzerland, 4410