Home › Bladder Cancer › NCT03193970
Measuring Surgical Recovery After Radical Cystectomy
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: 1\. Bladder cancer patients undergoing radical cystectomy at the MD Anderson Cancer Center and the collaborating centers. Exclusion Criteria: N/A
About the study
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.
What is being tested
- Post-Operative Recovery Registry (behavioral)
Sponsor: M.D. Anderson Cancer Center · Participants: 2,000 · Started: Apr 30, 2015
Contact the study team
- Neema Navai, MD · Phone: 713-792-3950
Official record on ClinicalTrials.gov — NCT03193970
Locations in the U.S.
| California | Stanford University, Stanford (Not yet recruiting) |
| Georgia | Emory University, Atlanta |
| Illinois | University of Chicago, Chicago |
| Kansas | University of Kansas Medical Center, Lawrence |
| Maryland | John Hopkins Medical Institutions, Baltimore |
| Michigan | Spectrum Health Medical Group, Grand Rapids (Not yet recruiting) |
| New York | Winthrop University Hospital, Mineola (Not yet recruiting) University of Rochester, Rochester |
| Texas | University of Texas - Southwestern, Dallas University of Texas MD Anderson Cancer Center, Houston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.