Zenapro™ Hybrid Hernia Repair Device for Ventral Hernia Repair

NCT01784822 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 63

Last updated 2017-06-15

No results posted yet for this study

Summary

The objective this study is to collect post-market data on the performance of the Zenapro™ Hybrid Hernia Repair Device when used to reinforce or bridge the abdominal wall for the repair of ventral hernias.

Conditions

  • Ventral Hernias

Interventions

DEVICE

Zenapro™ Hybrid Hernia Repair Device

Device will be placed during open or laparoscopic hernia repair.

Sponsors & Collaborators

  • Cook Group Incorporated

    lead INDUSTRY

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-02-28
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • United States

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 NCT01784822 on ClinicalTrials.gov