Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Measuring Surgical Recovery After Radical Cystectomy
NCT03193970 · View on ClinicalTrials.gov ↗
Study 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.
Conditions Studied
Interventions
- BEHAVIORAL Post-Operative Recovery Registry
Study Locations (11)
California
- University of California - San Francisco — San Francisco
- Stanford University — Stanford
New York
- Winthrop University Hospital — Mineola
- University of Rochester — Rochester
Texas
- University of Texas - Southwestern — Dallas
- University of Texas MD Anderson Cancer Center — Houston
Georgia
- Emory University — Atlanta
Illinois
- University of Chicago — Chicago
Kansas
- University of Kansas Medical Center — Lawrence
Maryland
- John Hopkins Medical Institutions — Baltimore
Michigan
- Spectrum Health Medical Group — Grand Rapids
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 2,000 participants |
| Start Date | 2015-04-30 |
| Est. Completion | 2034-12-31 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03193970
The ClinicalTrials.gov registry entry for NCT03193970 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 2,000 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is M.D. Anderson Cancer Center, which has 2,992 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Bladder Cancer appearing as the primary indexed condition, and to 1 intervention — of which Post-Operative Recovery Registry is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03193970 reports 11 study locations spanning 8 distinct geographic areas — top geographies include California, New York, Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03193970 about?
NCT03193970 is a clinical study titled "Measuring Surgical Recovery After Radical Cystectomy". 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 clin...
What is the current status of trial NCT03193970?
This trial is currently recruiting. The enrollment target is 2,000 participants. The study started on 2015-04-30. Estimated completion is 2034-12-31.
What conditions does trial NCT03193970 study?
This clinical trial studies the following conditions: Bladder Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03193970?
The interventions under investigation include: Post-Operative Recovery Registry (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03193970?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,992 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03193970 being conducted?
This trial has 11 study locations across California, Georgia, Illinois, Kansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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