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| Sponsors and Collaborators: |
National Center for Research Resources (NCRR) Columbia University |
| Information provided by: | National Center for Research Resources (NCRR) |
| ClinicalTrials.gov Identifier: | NCT00005101 |
Purpose
OBJECTIVES:
I. Determine the possible causes of bone loss in premenopausal or perimenopausal women.
| Condition |
|
Osteoporosis |
| MedlinePlus related topics: | 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.
Eligibility
| 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--
Contacts and Locations| United States, New York | |||||
| Columbia University College of Physicians and Surgeons | |||||
| New York, New York, United States, 10032 | |||||
| National Center for Research Resources (NCRR) |
| Columbia University |
| Study Chair: | Elizabeth Shane | Columbia University |
More Information
| Study ID Numbers: | NCRR-M01RR00645-2738, CPMC-IRB-8414, CPMC-GCRC-2738 |
| First Received: | April 6, 2000 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00005101 |
| Health Authority: | United States: Federal Government |
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