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Sponsors and Collaborators: |
National Center for Research Resources (NCRR) Columbia University |
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Information provided by: | National Center for Research Resources (NCRR) |
ClinicalTrials.gov Identifier: | NCT00005101 |
OBJECTIVES:
I. Determine the possible causes of bone loss in premenopausal or perimenopausal women.
Condition |
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Osteoporosis |
Study Type: | Observational |
Study Design: | Screening |
Study Start Date: | February 1998 |
PROTOCOL OUTLINE: Patients undergo physical examination and complete history with emphasis on risk factors for osteoporosis and screening for occult secondary causes of osteoporosis through blood serum and 24 hour urine collection.
Patients with more than 6 months since prior bone mineral density measurements or who did not receive measurements at participating center, undergo dual energy x-ray absorptiometry over 30 minutes for bone mineral density measurements.
Ages Eligible for Study: | 16 Years to 54 Years |
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
PROTOCOL ENTRY CRITERIA:
--Disease Characteristics--
OR
--Prior/Concurrent Therapy--
--Patient Characteristics--
United States, New York | |
Columbia University College of Physicians and Surgeons | |
New York, New York, United States, 10032 |
Study Chair: | Elizabeth Shane | Columbia University |
Study ID Numbers: | NCRR-M01RR00645-2738, CPMC-IRB-8414, CPMC-GCRC-2738 |
Study First Received: | April 6, 2000 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00005101 |
Health Authority: | United States: Federal Government |
disease-related problem/condition osteoporosis rare disease |
Musculoskeletal Diseases Rare Diseases Osteoporosis Bone Diseases, Metabolic Bone Diseases |