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Zoledronate in Treating Patients With Solid Tumors That Have Spread to the Bone
NCT00003884 · View on ClinicalTrials.gov ↗
Study Summary
RATIONALE: Zoledronate may help to relieve some of the symptoms caused by bone metastases. It is not yet known if zoledronate is more effective than no further therapy in relieving symptoms of bone metastases or preventing disease progression. PURPOSE: Randomized phase III trial to determine the effectiveness of zoledronate in treating patients who have solid tumors that have spread to the bone.
Conditions Studied
Interventions
- PROCEDURE quality-of-life assessment
- DRUG zoledronic acid
Study Locations (20)
California
- Columbia South Valley Hospital — Gilroy
- Pacific Shores Medical Group — Long Beach
- Veterans Affairs Medical Center - West Los Angeles — Los Angeles
- Jonsson Comprehensive Cancer Center, UCLA — Los Angeles
- Southwest Cancer Care — Poway
- Cancer and Blood Institute of the Desert — Rancho Mirage
Alabama
- SORRA Research Center — Birmingham
- Brookwood ACCC — Birmingham
- University of Alabama Comprehensive Cancer Center — Birmingham
Florida
- Veterans Affairs Medical Center - Miami — Miami
- Oncology-Hematology Group of South Florida — Miami
- H. Lee Moffitt Cancer Center and Research Institute — Tampa
Colorado
- Oncology Clinic, P.C. — Colorado Springs
- Veterans Affairs Medical Center - Denver — Denver
Arkansas
- Highlands Oncology Group — Springdale
District of Columbia
- Vincent T. Lombardi Cancer Research Center, Georgetown University — Washington D.C.
Georgia
- American Medical Research Institute, Inc. — Atlanta
Illinois
- Oncology Care Center - Belleville — Belleville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 1998-08 |
| Est. Completion | 2001-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00003884
The ClinicalTrials.gov registry entry for NCT00003884 describes a study currently listed as completed. It is categorized as Phase 3, 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 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis, which has 60 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 5 conditions, with Lung Cancer appearing as the primary indexed condition, and to 2 interventions — of which quality-of-life assessment 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: NCT00003884 reports 20 study locations spanning 10 distinct geographic areas — top geographies include California, Alabama, 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 NCT00003884 about?
NCT00003884 is a clinical study titled "Zoledronate in Treating Patients With Solid Tumors That Have Spread to the Bone". RATIONALE: Zoledronate may help to relieve some of the symptoms caused by bone metastases. It is not yet known if zoledronate is more effective than no further therapy in relieving symptoms of bone metastases or preventing disease progression. PURPOSE: Randomized phase III trial to determine the ef...
What is the current status of trial NCT00003884?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 600 participants. The study started on 1998-08. Estimated completion is 2001-01.
What conditions does trial NCT00003884 study?
This clinical trial studies the following conditions: Lung Cancer, Pain, Metastatic Cancer, Unspecified Adult Solid Tumor, Protocol Specific, Hypercalcemia of Malignancy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00003884?
The interventions under investigation include: quality-of-life assessment (PROCEDURE), zoledronic acid (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00003884?
This trial is sponsored by Novartis, which has 60 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00003884 being conducted?
This trial has 20 study locations across Alabama, Arkansas, California, Colorado, District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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