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NCT04947202: SAFIL_MESH

Clinical Study on the Safety of SAFIL® MESH

Completed Last updated 24 January 2022
What this trial tests

trial testing Hernioplasty in Abdominal Wall Defect in 152 participants. Completed in 30 November 2021.

Timeline
1 July 2021
Primary endpoint
30 November 2021
30 November 2021

Quick facts

Lead sponsorAesculap AG
StatusCompleted
Study typeOBSERVATIONAL
Enrollment152
Start date1 July 2021
Primary completion30 November 2021
Estimated completion30 November 2021
Sites2 locations across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Aesculap AG — full company profile →

Who can join

Eligibility, any sex, with Abdominal Wall Defect or Ventral Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Abdominal Wall Defect

Currently open trials in the same condition.

Other Aesculap AG trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04947202.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing