NCT Number: NCT00079924
Effects of Teriparatide in Postmenopausal Women With Osteoporosis
Effects of Teriparatide in Postmenopausal Women Previously Treated with Alendronate or Raloxifene.
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Notify MeKey information
Conditions
Age range
50 year and older
Sex eligibility
Female
Study type
Interventional
Phase
Phase 4
Primary location
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM - 5PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Birmingham, Alabama, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Postmenopausal women aged at least 50 years
- A previous clinical diagnosis of osteoporosis
- At high risk for fracture
- Current therapy for at least 18 months prior to study entry with either raloxifene HCl or alendronate Na
Exclusion criteria
- History of metabolic bone disease other than osteoporosis
- History of malignant neoplasm within the last 5 years except for superficial basal cell carcinoma or squamous cell carcinoma
Treatment and study plan
aldrenodate
DrugRaloxifene
DrugPrimary outcomes
-
Change in calcium values after beginning teriparatide
Secondary outcomes
-
Frequency of hypercalcemia, various calcium assessments, change in bone mineral density and tests of bone formation and resorption
Sponsors and collaborators
Lead sponsor
Eli Lilly and Company
Industry
Registry information
Official study title
Effects of Teriparatide in Postmenopausal Women With Osteoporosis Previously Treated With Alendronate or Raloxifene
Important dates
- Study start
- 2004
- Study completion
- 2007
- First posted
- Mar 19, 2004
- Registry last updated
- May 25, 2007
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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