CompletedNot Applicable

The SymCHro - Observational Registry Study for Symbotex™ Composite Mesh in Ventral Hernia Repair

France100 participantsStarted 2014-06-25

Plain-language 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 surgeries by open or laparoscopic approach, according to the Instruction for use (IFU).

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 Criteria: * No exclusion criteria outside the product IFU

What they're measuring

Incidence of Peri-operative and Post-operative Complications

Timeframe: Various (measured at 1 month, 1 Year & 2 Year)

Trial details

NCT IDNCT02206828

SponsorMedtronic - MITG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2017-05-22

Results submitted2018-09-04

View on ClinicalTrials.gov More Ventral Incisional Hernia trials