Effects of Endometriosis on Bone Mineral Density
Endometriosis
About this trial
This is an observational trial for Endometriosis focused on measuring Endometriosis, Bone Mineral Density, Osteopenia, Osteoporosis, DEXA Scan, Menopause, Screening, Healthy Volunteer, HV
Eligibility Criteria
INCLUSION CRITERIA: Regularly cycling women between the ages of 40 and 50 with surgically documented endometriosis (preferably biopsy proven, but unequivocal operative reports may allow inclusion). OR Regularly cycling women between the ages of 40 and 50 who are healthy volunteers. Women will be matched by ethnicity, by BMI within 5 kg/M(2), and by age (at the time of DEXA) in two groups: 40 - 45 years and 45 - 50 years. EXCLUSION CRITERIA: Women who are pregnant or lactating or who have abnormalities in the medical history or screening laboratory tests that might contribute to abnormal BMD (e.g. hypercalcemia, renal failure) will not be enrolled We will not include women who currently or have previously taken medications known to affect bone mineral density (e.g. thyroid hormone suppression, supraphysiologic glucocorticoids, GnRH, dilantin) or those that suggest menstrual abnormalities (fertility drugs), but we will consider other prescription drug use on a case-by-case basis.
Sites / Locations
- National Institutes of Health Clinical Center, 9000 Rockville Pike