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

Completed

Conditions studied: Abdominal Wall Defects

In brief

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

Key facts

Study ID

NCT01214252

Run by

Medtronic - MITG

People needed

343

Starts

2010-10-01

Expected to finish

2012-01-01

Last updated by the study team

2014-05-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Equal or over 18 years of age
• Had undergone surgical repair or reconstruction of abdominal wall defects, ventral hernias or incisional hernias using Permacol Surgical Implant.
• At least 12 months of follow-up post date of surgery (-30 days)
• Undergone open or laparoscopic repairs

You may not qualify if…

• Had undergone inguinal, parastomal, diaphragmatic or paraesophageal/hiatal hernia repair
• Any prior use of Permacol in abdominal wall repair

Where it is running

• Annie Choi — Bedford, Massachusetts, United States

Full record on ClinicalTrials.gov

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