Status and phase
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About
To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture
Sex
Ages
Volunteers
Inclusion criteria
Male and Female aged > 55 Low trauma hip fracture up to 90 days Be willing to submit to periodic bone mineral density radiographic studies of the spine & 24 hr urine collection Written informed consent
Exclusion criteria
Primary purpose
Allocation
Interventional model
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Central trial contact
Giselle Charrette, RN CONc; Richard Kremer, MD PhD
Data sourced from clinicaltrials.gov
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