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
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
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 osteoporosis
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
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