Overview
The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.
Status:
Unknown status
Unknown status
Trial end date:
2007-04-01
2007-04-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracturePhase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
McGill University Health Center
McGill University Health Centre/Research Institute of the McGill University Health CentreCollaborator:
Merck Frosst Canada Ltd.Treatments:
Alendronate
Criteria
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:
- Disorders known to affect bone metabolism Not taking bisphosphonates within last 6
months Drugs known to interfere with calcium metabolism within the lats 6 months prior
to hip fracture serum calcium> 2.65 mmol/L Treatment with any investigational drug
within the last 30 days