Clinical Trials Directory

Trials / Completed

CompletedNCT02908061

A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia

A Prospective, Randomized Trial of Preventive Mesh Placement at the Time of Radical Cystectomy to Reduce the Chances of Developing a Parastomal Hernia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
178 (actual)
Sponsor
Memorial Sloan Kettering Cancer Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
PROCEDURESurgery Radical CystectomyAll surgeries will be performed in an open or laparoscopic fashion.
PROCEDUREUltrapro meshSurgery Mesh Placement. All surgeries will be performed in an open or laparoscopic fashion.

Timeline

Start date
2016-08-01
Primary completion
2026-03-25
Completion
2026-03-25
First posted
2016-09-20
Last updated
2026-03-30

Locations

7 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT02908061. Inclusion in this directory is not an endorsement.

A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia (NCT02908061) · Clinical Trials Directory