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NCT00097812 · ClinicalTrials.gov registry record · Phase 3
Switching Osteoporosis Patients Currently on Oral Bisphosphonate to Zoledronic Acid
A Phase 3 study, sponsored by Novartis Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 220
- Enrollment target
NCT00097812: Completed Phase 3 study, sponsored by Novartis Pharmaceuticals.
NCT00097812 is a Phase 3 study that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 220 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00097812, a Phase 3 study, has completed, sponsored by Novartis Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 220 participants
- Enrollment target
Study Summary
The purpose of this study is to assess bone mineral density in patients switching from an oral bisphosphonate to zoledronic acid, compared to those staying on the oral bisphosphonate.
Interventions
- DRUG zoledronic acid
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 220 participants |
| Start Date | 2004-05 |
| Est. Completion | 2005-12 |
| Phase | Phase 3 |
What the finished NCT00097812 record still lists
NCT00097812 is an interventional study that assigns participants to a tested intervention. The registered 220 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (72% lower).
The record links to 0 conditions, and to 1 intervention - of which zoledronic acid is the first listed.
NCT00097812 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00097812 about?
NCT00097812 is a clinical study titled "Switching Osteoporosis Patients Currently on Oral Bisphosphonate to Zoledronic Acid". The purpose of this study is to assess bone mineral density in patients switching from an oral bisphosphonate to zoledronic acid, compared to those staying on the oral bisphosphonate.
What is the current status of trial NCT00097812?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 220 participants. The study started on 2004-05. Estimated completion is 2005-12.
What interventions are being tested in trial NCT00097812?
The interventions under investigation include: zoledronic acid (DRUG).
Who is sponsoring clinical trial NCT00097812?
This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00097812's enrollment target sits among peer trials
220 1318th of 2000 higher than 672 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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