Ignite Creation Date:
2024-10-26 @ 3:35 PM
Last Modification Date:
2024-10-26 @ 3:35 PM
Study NCT ID:
NCT06511414
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-07-16
Brief Title:
Effect of Duramesh on Hernia Formation After Ileostomy Closure Randomized Controlled Trial
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Effect of Duramesh on Hernia Formation After Ileostomy Closure Randomized Controlled Trial
Status:
RECRUITING
Status Verified Date:
2024-07
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Diverting ileostomy is frequently utilized to protect high-risk anastomoses though it is not shown to reduce the leak rate it may reduce the severe consequences of an anastomotic leak Ileostomy will be reversed with restoration of continuity in majority of patients Stoma site incisional hernias after ileostomy closure are complex hernias that can be associated with abdominal pain discomfort and a diminished quality of life Duramesh non-absorbable polypropylene suture is a hollow core microporous cylindrical suture made off in polypropylene filaments that are loosely braided and bonded to each other with heat and pressure The Aim of this study is to evaluate Duramesh suture vs standard closure on rates of hernia formation after ileostomy closure
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None