findmyKOL
Clinical trialNCT02908061CompletedPhase 3Interventional

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

SponsorMemorial Sloan Kettering Cancer CenterEnrollment178Radical Cystectomy
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

7 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Memorial Sloan Kettering Basking Ridge (consent and Follow-Up Only)

    Basking Ridge, New Jersey, United States

  • Memorial Sloan Kettering Monmouth (consent and Follow-Up Only)

    Middletown, New Jersey, United States

  • Memorial Sloan Kettering Bergen (consent and Follow-Up Only)

    Montvale, New Jersey, United States

  • Memorial Sloan Kettering Commack (consent and Follow-Up Only)

    Commack, New York, United States

  • Memorial Sloan Kettering Westchester (consent and Follow-Up Only)

    Harrison, New York, United States

  • Memorial Sloan Kettering Cancer Center (all Protocol Activities)

    New York, New York, United States

  • Memorial Sloan Kettering Nassau (consent Only and Follow Up)

    Uniondale, New York, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Aug 2016
Primary completion
25 Mar 2026
Completion
25 Mar 2026
Last update posted
30 Mar 2026
Registered enrollment
178
Registry id
NCT02908061
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.