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A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia
NCT02908061 · View on ClinicalTrials.gov ↗
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 Studied
Interventions
- PROCEDURE Surgery Radical Cystectomy
- PROCEDURE Ultrapro mesh
Study Locations (7)
New York
- Memorial Sloan Kettering Commack (Consent and follow-up only) — Commack
- Memorial Sloan Kettering Westchester (Consent and follow-up only) — Harrison
- Memorial Sloan Kettering Cancer Center (All Protocol Activities) — New York
- Memorial Sloan Kettering Nassau (Consent only and Follow Up) — Uniondale
New Jersey
- Memorial Sloan Kettering Basking Ridge (Consent and follow-up only) — Basking Ridge
- Memorial Sloan Kettering Monmouth (Consent and follow-up only) — Middletown
- Memorial Sloan Kettering Bergen (Consent and follow-up only) — Montvale
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 178 participants |
| Start Date | 2016-08 |
| Est. Completion | 2026-08 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02908061
The ClinicalTrials.gov registry entry for NCT02908061 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 178 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 2,280 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Radical Cystectomy appearing as the primary indexed condition, and to 2 interventions — of which Surgery Radical Cystectomy is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT02908061 reports 7 study locations spanning 2 distinct geographic areas — top geographies include New York, New Jersey. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT02908061 about?
NCT02908061 is a clinical study titled "A Study to Determine if Mesh Placement During Bladder Surgery Can Reduce the Chances of Developing a Hernia". 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.
What is the current status of trial NCT02908061?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 178 participants. The study started on 2016-08. Estimated completion is 2026-08.
What conditions does trial NCT02908061 study?
This clinical trial studies the following conditions: Radical Cystectomy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT02908061?
The interventions under investigation include: Surgery Radical Cystectomy (PROCEDURE), Ultrapro mesh (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT02908061?
This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 2,280 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT02908061 being conducted?
This trial has 7 study locations across New Jersey, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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