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Sponsored by: |
Nycomed |
---|---|
Information provided by: | Nycomed |
ClinicalTrials.gov Identifier: | NCT00515593 |
The objectives of the study are
Condition | Intervention |
---|---|
Postmenopause Osteoporosis |
Drug: Parathyroid hormone (PTH) (Preotact) |
Study Type: | Observational |
Study Design: | Case-Only, Prospective |
Official Title: | Non-Interventional Open Single Arm, Multicentre Study to Observe the Use of Preotact in Patients With Severe Postmenopausal Osteoporosis |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Patients with severe postmenopausal osteoporosis
Inclusion Criteria:
Responsible Party: | Nycomed ( Nycomed ) |
Study ID Numbers: | FP-004-DE |
Study First Received: | August 13, 2007 |
Last Updated: | March 17, 2009 |
ClinicalTrials.gov Identifier: | NCT00515593 History of Changes |
Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
osteoporosis postmenopausal women Severe postmenopausal osteoporosis |
Musculoskeletal Diseases Osteoporosis, Postmenopausal Quality of Life Osteoporosis |
Bone Diseases, Metabolic Hormones Bone Diseases |
Musculoskeletal Diseases Osteoporosis, Postmenopausal Osteoporosis Bone Diseases, Metabolic Bone Diseases |