NCT02908061View on ClinicalTrials.gov

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

PHASE3Active, not recruitingINTERVENTIONAL
Enrollment

178

Participants

Timeline

Start Date

August 31, 2016

Primary Completion Date

August 31, 2026

Study Completion Date

August 31, 2026

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.

Trial Locations (7)

10065

Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York

10604

Memorial Sloan Kettering Westchester (Consent and follow-up only), Harrison

11553

Memorial Sloan Kettering Nassau (Consent only and Follow Up), Uniondale

07920

Memorial Sloan Kettering Basking Ridge (Consent and follow-up only), Basking Ridge

07748

Memorial Sloan Kettering Monmouth (Consent and follow-up only), Middletown

07645

Memorial Sloan Kettering Bergen (Consent and follow-up only), Montvale

Unknown

Memorial Sloan Kettering Commack (Consent and follow-up only), Commack

All Listed Sponsors
lead

Memorial Sloan Kettering Cancer Center

OTHER

NCT02908061 - A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia | Biotech Hunter | Biotech Hunter