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Spots Global Cancer Trial Database for Measuring Surgical Recovery After Radical Cystectomy

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: Measuring Surgical Recovery After Radical Cystectomy

Official Title: Measuring Surgical Recovery After Radical Cystectomy

Study ID: NCT03193970

Conditions

Bladder Cancer

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

Useful links and downloads for this trial

Clinicaltrials.gov

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