Status:
COMPLETED
The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Ventral Hernia Repair
Lead Sponsor:
Medtronic - MITG
Conditions:
Ventral Incisional Hernia
Eligibility:
All Genders
18+ years
Brief Summary
The aim of this Observational Registry Study is to assess the short- and long-term clinical outcomes following the use of Symbotex™ Composite Mesh in primary and incisional abdominal wall hernia surge...
Detailed Description
This is an observational multicenter registry study. One hundred consecutive, adult patients scheduled for primary and incisional abdominal wall hernia surgeries using Symbotex™ Composite Mesh will be...
Eligibility Criteria
Inclusion
- The first one hundred consecutive adult patients scheduled for primary and incisional abdominal wall hernia surgery by Club Hernie members surgeons using Symbotex™Composite Mesh ;- All patients regardless of gender ≥ 18 years of age presenting with ventral hernias.
- Patients will be informed by surgeon with a written information notice of the nature of the observational registry study.
Exclusion
- No exclusion criteria outside the product IFU
Key Trial Info
Start Date :
June 25 2014
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 22 2017
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT02206828
Start Date
June 25 2014
End Date
May 22 2017
Last Update
January 14 2025
Active Locations (1)
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1
Club Hernie association represented by Dr Gillion, in his capacity as President
Montrouge, France, 92120