Clinical trial
Safety and Efficacy Trial With Zoledronic Acid for the Treatment of Paget's…
NCT00051636 · Novartis Pharmaceuticals, Industry · Completed
Key facts
| NCT number | NCT00051636 |
|---|---|
| Title | Safety and Efficacy Trial With Zoledronic Acid for the Treatment of Paget's Disease of Bone, Including an Extended Observation Period |
| Official title | Randomized, Double-blind, Safety and Efficacy Trial With Intravenous Zoledronic Acid for the Treatment of Paget's Disease of Bone Using Risedronate as a Comparator, Including an Extended Observational Period |
| Lead sponsor | Novartis Pharmaceuticals, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Paget's Disease of Bone |
| Intervention type | Dietary Supplement, Drug |
| Interventions | Zoledronic Acid, Risedronate, Placebo to Risedronate, Placebo to Zoledronic Acid, Calcium and Vitamin D |
| Enrollment | 172 |
| Start date | Jan 1, 2001 |
| Primary completion | Mar 1, 2004 |
| Completion | Apr 1, 2011 |
| First posted | Jan 15, 2003 |
| Last update posted | May 15, 2012 |
| Countries | Australia, Canada, New Zealand, Spain, United Kingdom, United States |
At a glance
- 10–99 Study sites
- Yes Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: