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

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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.


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
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Des Moines, IA
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Augusta, GA
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Decatur, GA
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Denver, CO
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Duncansville, Pennsylvania 16635
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Erie, PA
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Eugene, OR
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Houston, TX
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Indianapolis, IN
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Laguna Woods, CA
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Madison, WI
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Miami, FL
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Mission Viejo, California 92691
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Mission Viejo, CA
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Mount Pleasant, South Carolina 29464
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Mount Pleasant, SC
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Santa Clarita, California 91350
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