A Study of Ibandronate (Boniva) to Evaluate Satisfaction in Women With Post-Menopausal Osteoporosis or Osteopenia
Status: | Completed |
---|---|
Conditions: | Osteoporosis, Osteoporosis, Postmenopausal Syndrome, Gastrointestinal |
Therapuetic Areas: | Endocrinology, Gastroenterology, Rheumatology |
Healthy: | No |
Age Range: | Any |
Updated: | 8/3/2016 |
Start Date: | June 2004 |
End Date: | April 2006 |
A Prospective, Open-Label, Multi-Center, Two-Part Study to Investigate Patient Satisfaction With Monthly Dosed Ibandronate Therapy in Women With Post-Menopausal Osteoporosis or Osteopenia Transitioned From Once-Weekly Alendronate or Risendronate
This study will investigate participant satisfaction (including compliance, preference,
tolerability) with once-monthly Bonviva in women with post-menopausal osteoporosis or
osteopenia transitioned from once-weekly alendronate or risedronate. The anticipated time on
study treatment is 6 months, and the target sample size is 1776 individuals.
tolerability) with once-monthly Bonviva in women with post-menopausal osteoporosis or
osteopenia transitioned from once-weekly alendronate or risedronate. The anticipated time on
study treatment is 6 months, and the target sample size is 1776 individuals.
Inclusion Criteria:
- Women who had been receiving once-weekly alendronate or risedronate for treatment or
prevention of post-menopausal osteoporosis for greater than or equal to (>=) 3 months
Exclusion Criteria:
- Inability to stand or sit upright for >=60 minutes
- Hypersensitivity to bisphosphonates
- Inability to swallow a tablet whole
- Malignant disease diagnosed within previous 10 years (except resected basal cell
cancer).
We found this trial at
132
sites
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