Measuring Surgical Recovery After Radical Cystectomy
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
The intent of this study is to establish a registry of post-surgical outcomes in patients undergoing radical cystectomy at MD Anderson Cancer Center and the collaborating institutions. The goals of this initiative are to obtain a detailed baseline of multiple patient-reported outcomes (PRO) and clinician-reported outcomes (CRO) as well as various presenting conditions associated with them, so that future quality improvement interventions can be evaluated accurately as to their relative contribution to improved outcomes.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Pacjenci z rakiem pęcherza moczowego, którym planuje się usunięcie pęcherza moczowego w MD Anderson Cancer Center lub współpracujących ośrodkach
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- August 19, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (10)
Stanford University
Stanford, United States
Emory University
Atlanta, United States
University of Chicago
Chicago, United States
University of Kansas Medical Center
Lawrence, United States
John Hopkins Medical Institutions
Baltimore, United States
Spectrum Health Medical Group
Grand Rapids, United States
Winthrop University Hospital
Mineola, United States
University of Rochester
Rochester, United States
University of Texas - Southwestern
Dallas, United States
University of Texas MD Anderson Cancer Center
Houston, United States
Trial contact
Neema Navai, MD
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/20/2026.
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