Clinical trial
DIVA Study - A Study of Different Regimens of Intravenous Administration of…
NCT00048074 · Hoffmann-La Roche, Industry · Completed
Key facts
| NCT number | NCT00048074 |
|---|---|
| Title | DIVA Study - A Study of Different Regimens of Intravenous Administration of Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis |
| Official title | A Randomized, Double-blind Study Comparing the Effect of Different Treatment Regimens of Intravenous Bonviva on Lumbar Bone Mineral Density in Women With Osteoporosis |
| Lead sponsor | Hoffmann-La Roche, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Post Menopausal Osteoporosis |
| Intervention type | Drug |
| Interventions | ibandronate [Bonviva/Boniva] |
| Enrollment | 1,395 |
| Start date | Jun 1, 2002 |
| Primary completion | May 1, 2005 |
| Completion | May 1, 2005 |
| First posted | Oct 25, 2002 |
| Last update posted | Feb 3, 2016 |
| Countries | Australia, Belgium, Canada, Czechia, Denmark, France, Germany, Hungary, Italy, Mexico, Norway, Poland and 4 more |
At a glance
- 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: