MedTrace Logo

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

NCT02206828 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2025-01-14

Study results available
· View outcomes & findings →

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).

Conditions

  • Ventral Incisional Hernia

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Principal Investigators

  • Jean-François Gillion · ICMJE

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-06-25
Primary Completion
2017-05-22
Completion
2017-05-22

Countries

  • France

Study Locations

More Related Trials

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 NCT02206828 on ClinicalTrials.gov