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Measuring Surgical Recovery in Participants Undergoing Radical Cystectomy
Trial Status: active
This trial studies surgical recovery in participants undergoing radical cystectomy. Measuring surgical recovery may help in obtaining a detailed baseline of all critical patient‐reported outcome and clinician‐reported outcome elements of post‐operative recovery.
Inclusion Criteria
All patients presenting to MD Anderson and the collaborating centers undergoing radical cystectomy between 1/1/2015 and 12/31/2034
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03193970.
I. To establish a registry of post‐surgical outcomes in patients undergoing radical cystectomy at MD Anderson Cancer Center and the collaborating institutions.
II. 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.
OUTLINE:
Establish a registry of post-surgical outcomes in participants with bladder cancer undergoing radical cystectomy.
