Measuring Surgical Recovery After Radical Cystectomy
Summary
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.
Arms & interventions
- BehavioralPost-Operative Recovery Registry
Multi-institutional prospective database of patients with bladder cancer undergoing radical cystectomy.
Outcome measures
Primary
Post-Surgical Outcomes in Patients Undergoing Radical Cystectomy
Post-surgical outcomes determined from patient-reported assessment of symptom burden using the MD Anderson Symptom Inventory (MDASI-BLC form).
Time frame: 3 months
Eligibility criteria
Study locations (11)
University of California - San Francisco
San Francisco, California, 94143
Stanford University
Stanford, California, 94305
Emory University
Atlanta, Georgia, 30322
University of Chicago
Chicago, Illinois, 60637
University of Kansas Medical Center
Lawrence, Kansas, 66045
John Hopkins Medical Institutions
Baltimore, Maryland, 21205
Spectrum Health Medical Group
Grand Rapids, Michigan, 49503
Winthrop University Hospital
Mineola, New York, 11501
University of Rochester
Rochester, New York, 14611
University of Texas - Southwestern
Dallas, Texas, 75390
University of Texas MD Anderson Cancer Center
Houston, Texas, 77339