Measuring Surgical Recovery After Radical Cystectomy

INTRODUCTION

  • Org Study ID: PA15-0026
  • Secondary ID: N/A
  • NCT ID: NCT03193970
  • Sponsor: M.D. Anderson Cancer Center

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.

  • Overall Status
    Recruiting
  • Start Date
    April 30, 2015
  • Phase
  • Study Type
    Observational

PRIMARY OUTCOMES

Primary Outcome 1 - Measure:

Primary Outcome 1 - Timeframe: N/A

CONDITION

  • Bladder Cancer

ELIGIBILITY

Inclusion Criteria:
1. Bladder cancer patients undergoing radical cystectomy at the MD Anderson Cancer Center and the collaborating centers.
Exclusion Criteria:
N/A

Gender: All

Minimum Age: 18 Years

Maximum Age: N/A

Healthy Volunteers: No

OFFICIAL INFORMATION

Name: Neema Navai, MD

Role: Principal Investigator

Affiliation: M.D. Anderson Cancer Center

Overall Contact

Name: Neema Navai, MD

Phone: 713-792-3950

Email: nnavai@mdanderson.org

LOCATION

Facility Status Contact