A Retrospective Study Evaluating the Use of Permacol Surgical Implant in the Repair of Abdominal Wall Defects

NCT01214252 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 343

Last updated 2014-05-09

Study results available
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Summary

To evaluate short, mid and long term clinical outcomes associated with the use of Permacol in the treatment of abdominal wall defects.

Conditions

  • Abdominal Wall Defects

Interventions

DEVICE

Permacol Surgical Implant

Permacol Surgical Implant

Sponsors & Collaborators

  • Medtronic - MITG

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2011-09-30
Completion
2012-01-31

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 NCT01214252 on ClinicalTrials.gov