Effects of Anorexia Nervosa on Bone Mass in Adolescents
Anorexia Nervosa
About this trial
This is an interventional treatment trial for Anorexia Nervosa focused on measuring Anorexia Nervosa, Amenorrhea, Bone Mass, Growth hormone
Eligibility Criteria
Inclusion Criteria: Females Only with Anorexia Nervosa and Amenorrhea 12-18 years Normal-weight girls 12-18 years with no past or present history of an eating disorder Exclusion Criteria: Diseases affecting bone metabolism (including untreated thyroid disease, premature ovarian failure, diabetes, cancer, pituitary, renal disease or bone fracture within the past six months) Use of prescription medications affecting bone metabolism within three months Suicidality Psychosis Substance abuse Hematocrit <30 % Potassium <3.0 mmol/L Glucose <50 mg/dl.
Sites / Locations
- Massachusetts General Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Physiologic estrogen replacement
Placebo
Mature girls with anorexia nervosa (AN) (bone age 15 or greater): Transdermal estradiol (100 mcg) with cyclic progesterone (days 1-10 of each month). Immature girls with AN (bone age less than 15 years): Ethinyl estradiol (3.75 mcg daily for the first 6 months, 7.5 mcg daily for the next 6 months, and 11.25 mcg daily for the final 6 months of the study
Placebo patches or pills