What this study is
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's being tested
- Post-Operative Recovery Registry
Intervention · BEHAVIORAL
Multi-institutional prospective database of patients with bladder cancer undergoing radical cystectomy.
Study details
- Sponsor
- M.D. Anderson Cancer Center
- Conditions
- Bladder Cancer
- Enrolling
- 2,000 people
- Starts
- 2015-04-30
- Est. completion
- 2034-12-31
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Bladder cancer patients undergoing radical cystectomy at the MD Anderson Cancer Center and the collaborating centers.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (10)
10 open- Not yet recruiting
- Recruiting
University of Chicago
Chicago, Illinois, United States
- Gary D. Steinberg, MD · Contactgsteinbe@surgery.bsd.uchicago.edu
RecruitingUniversity of Kansas Medical Center
Lawrence, Kansas, United States
- Eugene Lee, MD · Contactelee@kumc.edu
RecruitingJohn Hopkins Medical Institutions
Baltimore, Maryland, United States
- Trinity Bivalacqua, MD, PhD · Contact
- Contacttbivala1@jhmi.edu
RecruitingSpectrum Health Medical Group
Grand Rapids, Michigan, United States
- Brian Lane, MD · ContactBrian.lane@spectrumhealth.org
Not yet recruitingWinthrop University Hospital
Mineola, New York, United States
- Anthony Corcoran, MD · ContactACorcoran@Winthrop.org
Not yet recruitingUniversity of Rochester
Rochester, New York, United States
- Edward Messing, MD · Contactedwardmessing@urmc.rochester.edu
RecruitingUniversity of Texas - Southwestern
Dallas, Texas, United States
- Yair Lotan, MD · ContactYair.Lotan@UTSouthwestern.edu
RecruitingUniversity of Texas MD Anderson Cancer Center
Houston, Texas, United States
- Neema Navai, MD · Contactnnavai@mdanderson.org
Recruiting
Study team
Sponsor
M.D. Anderson Cancer Center
Study ID PA15-0026
Principal investigator
Neema Navai, MD
M.D. Anderson Cancer Center
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.