Measuring Surgical Recovery After Radical Cystectomy
Recruiting now NCT03193970
Run by M.D. Anderson Cancer Center · for 18 and older · All sexes
What this study is about
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.
Who can join (things the study team will check)
✅ You may be able to join if…
- Bladder cancer patients undergoing radical cystectomy at the MD Anderson Cancer Center and the collaborating centers.
Where this trial is running
- University of California - San Francisco, San Francisco, California, United States
- Stanford University, Stanford, California, United States
- Emory University, Atlanta, Georgia, United States
- University of Chicago, Chicago, Illinois, United States
- University of Kansas Medical Center, Lawrence, Kansas, United States
- John Hopkins Medical Institutions, Baltimore, Maryland, United States
- Spectrum Health Medical Group, Grand Rapids, Michigan, United States
- Winthrop University Hospital, Mineola, New York, United States
- University of Rochester, Rochester, New York, United States
- University of Texas - Southwestern, Dallas, Texas, United States
- University of Texas MD Anderson Cancer Center, Houston, Texas, United States
Who to contact
Neema Navai, MD · 713-792-3950 · nnavai@mdanderson.org
It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT03193970.
Verify everything on the official ClinicalTrials.gov record. Page updated July 2026.