Spots Global Cancer Trial Database for Measuring Surgical Recovery After Radical Cystectomy
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Trial Identification
Brief Title: Measuring Surgical Recovery After Radical Cystectomy
Official Title: Measuring Surgical Recovery After Radical Cystectomy
Study ID: NCT03193970
Conditions
Interventions
Study Description
Brief 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.
Detailed Description:
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
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
Contact Details
Name: Neema Navai, MD
Affiliation: M.D. Anderson Cancer Center
Role: PRINCIPAL_INVESTIGATOR
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