A Study of Ibandronate (Bonviva) in Patients With Post-Menopausal Osteoporosis
| Status: | Completed |
|---|---|
| Conditions: | Osteoporosis, Osteoporosis, Postmenopausal Syndrome |
| Therapuetic Areas: | Endocrinology, Rheumatology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 8/3/2016 |
| Start Date: | March 2004 |
| End Date: | May 2005 |
A Randomized, Open-Label, Muti-Center Study to Investigate Patient Preference on Dosing in Women With Postmenopausal Osteoporosis Treated With Once-Monthly Ibandronate and Once-Weekly Alendronate. A Six Month, Two-Sequence, and Two-Period Crossover Study
This study will evaluate participant-reported preference for either ibandronate or a
comparator drug in women with postmenopausal osteoporosis. The anticipated time of study
treatment is 6 months, and the target sample size is 338 individuals.
comparator drug in women with postmenopausal osteoporosis. The anticipated time of study
treatment is 6 months, and the target sample size is 338 individuals.
Inclusion Criteria:
- Ambulatory women
- Diagnosis of post-menopausal osteoporosis
- Women who have never received bisphosphonate therapy, or who have discontinued daily
bisphosphonates at least 3 months prior to study entry
Exclusion Criteria:
- Inability to stand or sit in the upright position for greater than or equal to 60
minutes
- Allergy to bisphosphonates;
- Previous or current treatment with weekly or monthly bisphosphonates, or daily
bisphosphonates for the last 3 months prior to study entry
We found this trial at
50
sites
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