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Clinical Study on the Safety of SAFIL® MESH

NCT04947202 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 152

Last updated 2022-01-24

No results posted yet for this study

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

Conditions

  • Abdominal Wall Defect
  • Ventral Hernia
  • Abdominal Hernia
  • Fascial Hernia

Interventions

DEVICE

Hernioplasty

Hernioplasty is the repair of the defect using mesh patches.

Sponsors & Collaborators

  • B.Braun Surgical SA

    collaborator INDUSTRY

  • Aesculap AG

    lead INDUSTRY

Principal Investigators

  • Izaskun Badiola Bergara, Dr. · Hospital Galdakao-Usansolo

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2021-11-30
Completion
2021-11-30

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04947202 on ClinicalTrials.gov