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Local Bisphosphonate Effect on Recurrence Rate in Extremity Giant Cell Tumor of Bone
NCT03295981 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of the clinical study is to investigate whether the local delivery of bisphosphonate as a surgical adjuvant can decrease the chance of a giant cell tumor of bone coming back to the same location. The hypothesis is that the local administration of bisphosphonate will decrease the rate of the tumor returning compared to traditional aggressive surgical removal of the tumor.
Conditions Studied
Interventions
- DRUG Zoledronic Acid
Study Locations (16)
Massachusetts
- Massachusetts General Hospital — Boston
- Boston Children's Hospital — Boston
- Beth Israel Deaconess Medical Center — Boston
California
- University of California - Los Angeles — Los Angeles
Indiana
- Indiana University — Indianapolis
Iowa
- University of Iowa — Iowa City
Kansas
- University of Kansas — Overland Park
Maryland
- Johns Hopkins University Hospital — Baltimore
Missouri
- Saint Louis University — St Louis
North Carolina
- Wake Forest University — Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2018-05-03 |
| Est. Completion | 2028-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03295981
The ClinicalTrials.gov registry entry for NCT03295981 describes a study currently listed as recruiting. 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 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is St. Louis University, which has 35 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 Giant Cell Tumor of Bone appearing as the primary indexed condition, and to 1 intervention — of which Zoledronic Acid 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: NCT03295981 reports 16 study locations spanning 14 distinct geographic areas — top geographies include Massachusetts, California, Indiana. 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 NCT03295981 about?
NCT03295981 is a clinical study titled "Local Bisphosphonate Effect on Recurrence Rate in Extremity Giant Cell Tumor of Bone". The purpose of the clinical study is to investigate whether the local delivery of bisphosphonate as a surgical adjuvant can decrease the chance of a giant cell tumor of bone coming back to the same location. The hypothesis is that the local administration of bisphosphonate will decrease the rate of ...
What is the current status of trial NCT03295981?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 120 participants. The study started on 2018-05-03. Estimated completion is 2028-01.
What conditions does trial NCT03295981 study?
This clinical trial studies the following conditions: Giant Cell Tumor of Bone. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03295981?
The interventions under investigation include: Zoledronic Acid (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03295981?
This trial is sponsored by St. Louis University, which has 35 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03295981 being conducted?
This trial has 16 study locations across California, Indiana, Iowa, Kansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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