Overview

The Study of the Early Administration of Alendronate on Prevention of Bone Loss After Hip Fracture.

Status:
Unknown status
Trial end date:
2007-04-01
Target enrollment:
0
Participant gender:
All
Summary
To determine whether administration of Alendronate early is more effective than late in the prevention of osteoporosis following a hip fracture
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
McGill University Health Center
McGill University Health Centre/Research Institute of the McGill University Health Centre
Collaborator:
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