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Docetaxel and Gemcitabine in Treating Patients With Progressive Regional or Metastatic Bladder Cancer
NCT00004223 · View on ClinicalTrials.gov ↗
Study Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of docetaxel and gemcitabine in treating patients who have progressive regional or metastatic bladder cancer.
Conditions Studied
Interventions
- DRUG docetaxel
- DRUG gemcitabine hydrochloride
Study Locations (20)
Illinois
- Robert H. Lurie Comprehensive Cancer Center, Northwestern University — Chicago
- Veterans Affairs Medical Center - Lakeside Chicago — Chicago
- CCOP - Central Illinois — Decatur
- CCOP - Evanston — Evanston
- CCOP - Illinois Oncology Research Association — Peoria
- CCOP - Carle Cancer Center — Urbana
California
- Cancer Center and Beckman Research Institute, City of Hope — Duarte
- Veterans Affairs Medical Center - Palo Alto — Palo Alto
- Stanford University Medical Center — Stanford
Florida
- Veterans Affairs Medical Center - Gainsville — Gainesville
- Veterans Affairs Medical Center - Tampa (Haley) — Tampa
Georgia
- Emory University Hospital - Atlanta — Atlanta
- Veterans Affairs Medical Center - Atlanta (Decatur) — Decatur
Indiana
- Indiana University Cancer Center — Indianapolis
- Veterans Affairs Medical Center - Indianapolis (Roudebush) — Indianapolis
Arizona
- CCOP - Scottsdale Oncology Program — Scottsdale
Colorado
- CCOP - Colorado Cancer Research Program, Inc. — Denver
Delaware
- CCOP - Christiana Care Health Services — Wilmington
Trial Details
| Field | Value |
|---|---|
| Start Date | 2000-02-24 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00004223
The ClinicalTrials.gov registry entry for NCT00004223 describes a study currently listed as completed. It is categorized as Phase 2, 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. An enrollment target was not published in the registry record, which is common for early-stage or observational entries. The listed sponsor is Eastern Cooperative Oncology Group, which has 30 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Bladder Cancer appearing as the primary indexed condition, and to 2 interventions — of which docetaxel 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: NCT00004223 reports 20 study locations spanning 10 distinct geographic areas — top geographies include Illinois, California, Florida. 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 NCT00004223 about?
NCT00004223 is a clinical study titled "Docetaxel and Gemcitabine in Treating Patients With Progressive Regional or Metastatic Bladder Cancer". RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of docetaxel and gemcitabine in treating patients who have progressive r...
What is the current status of trial NCT00004223?
This trial is currently completed. It is a Phase 2 study. The study started on 2000-02-24.
What conditions does trial NCT00004223 study?
This clinical trial studies the following conditions: Bladder Cancer, Urethral Cancer, Transitional Cell Cancer of the Renal Pelvis and Ureter. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00004223?
The interventions under investigation include: docetaxel (DRUG), gemcitabine hydrochloride (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00004223?
This trial is sponsored by Eastern Cooperative Oncology Group, which has 30 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00004223 being conducted?
This trial has 20 study locations across Arizona, California, Colorado, Delaware, District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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