CompletedNot Applicable

Clinical Study on the Safety of SAFIL® MESH

Spain152 participantsStarted 2021-07-01

Plain-language summary

Observational, Retrospective, Multi-center Clinical Study on the Safety of SAFIL® MESH in Patients Undergoing Reinforcement of Soft Tissues After Abdominal Wall Surgery or Other Fascial Defects

Who can participate

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: * Patients operated between January 2019 - November 2020 for abdominal wall surgery or other fascial defects and received Safil® Mesh Exclusion Criteria: * No exclusion criteria have been set.

What they're measuring

Hernia rate

Timeframe: at one follow-up 12-30 months after initial intervention

Trial details

NCT IDNCT04947202

SponsorAesculap AG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2021-11-30

View on ClinicalTrials.gov More Abdominal Wall Defect trials