Transdermal Estrogen in Older Premenopausal Women With Anorexia Nervosa

Osteoporosis Clinical Trial

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Official title:

Transdermal Estrogen in Older Premenopausal Women With Anorexia Nervosa

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02475265
• Other study ID #: 2015P000463
• Secondary ID: R03DK106410
• Status: Completed
• Phase: Phase 2
• Start date: July 2015
• Est. completion date: July 30, 2018

Study information

• Verified date: July 2019
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Decreased bone strength is a common and serious medical problem present in many women with anorexia nervosa. Women with decreased bone strength are more likely to suffer broken bones than women with normal bone strength.

This study will investigate whether the use of transdermal estrogen can improve bone mineral density (BMD) and bone microarchitecture in women with anorexia nervosa anorexia nervosa when used for 6 months.

Description:

Anorexia nervosa (AN) is a prevalent psychiatric disorder affecting up to 1% of college-aged women in the US and an increasing number of women over 30 years of age. Among the many medical co-morbidities associated with AN, the most common is significant bone loss, which can persist despite weight recovery. Nearly 50% of women with AN have osteopenia with an additional 30% meeting WHO criteria for osteoporosis. Importantly, this severe bone loss is associated with an increased fracture risk. Nearly 30% of women with AN report a history of a fracture and a prospective study demonstrated a 7-fold increased risk of fracture in women with AN compared to age-matched controls. Because AN is a chronic disease that can persist despite psychiatric and nutritional counseling, the bone loss and increased fracture risk can persist and lead to lifelong morbidity. Therefore, finding a treatment for bone loss associated with AN is of critical importance.

This 6 month open-label study will investigate in women (ages 25 to 50 years old) with AN whether treatment with transdermal estrogen replacement will increase bone mineral density (BMD), improve parameters of bone microarchitecture as assessed by high-resolution peripheral quantitative computed tomography (HR-pQCT), and improve bone strength as estimated by microfinite element analysis.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 11
• Est. completion date: July 30, 2018
• Est. primary completion date: June 27, 2018
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 25 Years to 50 Years

Eligibility

Inclusion Criteria:

• Female; ages 25-50 years

• Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-V) psychiatric criteria for AN, including <85% of ideal body weight as defined by the 1983 Metropolitan Life Insurance Height and Weight Tables, and amenorrhea

• T-score of < -1.5 at spine or hip

• Treatment team or treatment professional in place for clinical treatment/monitoring during the study

Exclusion Criteria:

• Diseases known to affect bone metabolism, including untreated thyroid dysfunction, vitamin D deficiency, Cushing's syndrome, diabetes mellitus or renal insufficiency

• Personal history of venous or arterial clot

• History of stroke or myocardial infarction

• History of migraine headaches

• History of hypercoagulable disorder

• Personal history or history of a first-degree relative with breast cancer

• History of hereditary angioedema

• Any medication known to affect bone metabolism, including systemic glucocorticoids within three months of the baseline visit, depot medroxyprogesterone within 6 months of the baseline visit, oral bisphosphonates within one year of the baseline visit or intravenous (IV) bisphosphonates within three years of the baseline visit

• Bone fracture within the prior 12 months

• Serum potassium < 3.0 meq/L or serum alanine aminotransferase (ALT) > 3 times the upper limit of normal

• Fasting serum triglyceride level > 150 mg/dL

• Pregnant or breastfeeding

• Active substance abuse

Related Conditions & MeSH terms

• Anorexia
• Anorexia Nervosa
• Osteoporosis

Intervention

Drug:
• estradiol 0.045 mg/levonorgestrel 0.015mg

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Massachusetts General Hospital	National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percent Change in Bone Mineral Density (BMD) of Lumbar Spine by Dual Energy X-ray Absorptiometry (DXA)	Percent change in lumbar spine bone mineral density after six-months. Lumbar spine bone mineral density measured by dual energy x-ray absorptiometry.	6 months