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Recruiting Phase 3 Interventional

A Study of Surgical Techniques During Cystectomy

ClinicalTrials.gov ID: NCT06703476

Public ClinicalTrials.gov record NCT06703476. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 5:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Clinically Integrated Randomized Clinical Trial (RCT) of Modifications to Radical Cystectomy and Postoperative Care

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to look at two standard surgical techniques used during a radical cystectomy and see whether they influence outcomes such as length of stay in the hospital and infections after surgery. This trial will evaluate whether the following surgical methods influence outcomes: A ureteral stent is a thin tube that is placed in the ureter to drain urine from the kidney. Ureteral stents are often used to promote urine drainage after radical cystectomy, but may come at risk of urinary tract infection. Alvimopan is a standard drug used to promote return of bowel function following surgery. Doctors do not know whether alvimopan is beneficial in current clinical practice. The surgeon will decide whether participants will receive a stent and/or alvimopan, but if they are unsure what the best approach is, a surgical technique has been assigned by chance to them.

Study identification

NCT ID
NCT06703476
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Enrollment
530 participants

Conditions and interventions

Conditions

Interventions

Procedure · Drug

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 20, 2024
Primary completion
Oct 31, 2028
Completion
Oct 31, 2028
Last update posted
Jul 12, 2026

2024 – 2028

United States locations

U.S. sites
7
U.S. states
2
U.S. cities
7
Facility City State ZIP Site status
Memorial Sloan Kettering at Basking Ridge (Consent Only) Basking Ridge New Jersey 07920 Recruiting
Memorial Sloan Kettering Monmouth (Consent Only) Middletown New Jersey 07748 Recruiting
Memorial Sloan Kettering Bergen (Consent Only) Montvale New Jersey 07645 Recruiting
Memorial Sloan Kettering Suffolk-Commack (Consent Only) Commack New York 11725 Recruiting
Memorial Sloan Kettering Westchester (Consent Only) Harrison New York 10604 Recruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activites) New York New York 10065 Recruiting
Memorial Sloan Kettering Nassau (Consent Only) Rockville Centre New York 11553 Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06703476, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 12, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06703476 live on ClinicalTrials.gov.

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