Viewing Study NCT02908061


Ignite Creation Date: 2025-12-24 @ 1:10 PM
Ignite Modification Date: 2026-02-28 @ 2:50 AM
Study NCT ID: NCT02908061
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-09-19
First Post: 2016-09-09
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia
Sponsor: Memorial Sloan Kettering Cancer Center
Organization:

Study Overview

Official Title: A Prospective, Randomized Trial of Preventive Mesh Placement at the Time of Radical Cystectomy to Reduce the Chances of Developing a Parastomal Hernia
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2024-09
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: The purpose of this study is to compare any good and bad effects of using Ultrapro mesh along with the usual bladder removal surgery, versus having the usual bladder removal surgery without the use of the mesh.
Detailed Description: None

Study Oversight

Has Oversight DMC:
Is a FDA Regulated Drug?:
Is a FDA Regulated Device?:
Is an Unapproved Device?:
Is a PPSD?:
Is a US Export?:
Is an FDA AA801 Violation?: