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

NCT02908061 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 178

Last updated 2026-03-30

No results posted yet for this study

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

  • Radical Cystectomy

Interventions

PROCEDURE

Surgery Radical Cystectomy

All surgeries will be performed in an open or laparoscopic fashion.

PROCEDURE

Ultrapro mesh

Surgery Mesh Placement. All surgeries will be performed in an open or laparoscopic fashion.

Sponsors & Collaborators

Principal Investigators

  • Bernard Bochner, MD · Memorial Sloan Kettering Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2026-03-25
Completion
2026-03-25

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02908061 on ClinicalTrials.gov