Ignite Creation Date:
2025-12-25 @ 2:49 AM
Ignite Modification Date:
2025-12-30 @ 6:10 PM
Study NCT ID:
NCT01364233
Status:
COMPLETED
Last Update Posted:
2019-02-26
First Post:
2011-05-27
Is Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Safety Study of MotifMESH (cPTFE) in Abdominal Surgery
Sponsor:
Medline Industries
Organization:
Study Overview
Official Title:
A Prospective Outcome Study of Condensed Fenestrated PTFE Mesh (MotifMESH) in Non-sterile Abdominal Wall Defects
Status:
COMPLETED
Status Verified Date:
2019-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will monitor surgically repaired large abdominal hernias requiring condensed fenestrated polytetrafluoroethylene mesh (cPTFE).
Detailed Description:
cPTFEi s a mesh-like product designed to reduce associated post surgical complications.
Study Oversight
Has Oversight DMC:
False
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?: