ISRCTN79431254
Completed
Not Applicable
A randomised controlled study to compare the use of Permacol™ for repair of parastomal hernias with current treatment with either synthetic mesh or primary suture repair
Tissue Science Laboratories plc (UK)0 sites0 target enrollmentSeptember 21, 2004
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Tissue Science Laboratories plc (UK)
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients must have a symptomatic parastomal hernia; be aged over 18 (or the country applicable age of consent); if of child\-bearing age must have given a negative pregnancy test; give written informed consent; agree to be randomised.
Exclusion Criteria
- •Patients must not be taking part in another clinical study; not be suffering from an UNTREATED metabolic or systemic illness (e.g. diabetes or rheumatoid arthritis); not have a diagnosis of mentally limiting conditions such as Alzheimer's or mental retardation or be unable to understand all study requirements; not be allergic to any porcine or collagen products.
Outcomes
Primary Outcomes
Not specified
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