Expired Study
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Bedford, Massachusetts 01730


Purpose:

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


Criteria:

Inclusion Criteria: - 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 Exclusion Criteria: - Had undergone inguinal, parastomal, diaphragmatic or paraesophageal/hiatal hernia repair - Any prior use of Permacol in abdominal wall repair


NCT ID:

NCT01214252


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Bedford, Massachusetts 01730
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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