Study of Low Bone Mass in Premenopausal or Perimenopausal Women

Status Completed

Clinical Trial Summary

OBJECTIVES:

I. Determine the possible causes of bone loss in premenopausal or perimenopausal women.

Clinical Trial Description

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. ;

Study Design

Primary Purpose: Screening

Related Conditions & MeSH terms

Osteoporosis

Clinical Trial Details

NCT number	NCT00005101
Study type	Observational
Source	National Center for Research Resources (NCRR)
Contact
Status	Completed
Phase	N/A
Start date	February 1998

View Details

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