Overview
A Study to Compare the Efficacy of Alendronate With and Without Calcium or Calcium Alone In the Treatment of Osteoporosis in Postmenopausal Women (0217-088)(COMPLETED)
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
The purpose of this study is to see how well alendronate and calcium as compared to calcium alone increase bone density in postmenopausal women with osteoporosisPhase:
Phase 3Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Merck Sharp & Dohme Corp.Treatments:
Alendronate
Calcium
Calcium Carbonate
Calcium, Dietary
Criteria
Inclusion Criteria :- Patient is postmenopausal (or surgically menopausal) for at least 5 years.
- Patient must be diagnosed with osteoporosis
- Patient has spinal anatomy suitable for DEXA of the lumbar spine
Exclusion Criteria :
- Patient is receiving or has received treatment prior to randomization which might
influence bone turnover
- Patient has a history of or evidence for metabolic bone disease (other than
postmenopausal bone loss)
- Patient is receiving or is expected to receive during the course of the study any
medication (other than study medication) which might alter bone or calcium metabolism