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Clinical Trials/ACTRN12614000221651
ACTRN12614000221651
Not yet recruiting
未知

A randomised controlled trial evaluating the effects of biologic mesh for the prevention of parastomal hernias in patients undergoing colostomy, ileostomy, ileal, colonic or conduits

Dr. Peter Lee0 sites76 target enrollmentMarch 3, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Parastomal Hernias
Sponsor
Dr. Peter Lee
Enrollment
76
Status
Not yet recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 3, 2014
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Dr. Peter Lee

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older; undergoing colostomy, ileostomy, or ileal or colonic conduits; Patients fit for surgery; Informed consent attained.

Exclusion Criteria

  • Age less than 18 years; patients who have previously had mesh inserted to the site of stoma formation or those who cannot have mesh inserted; no informed consent.

Outcomes

Primary Outcomes

Not specified

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