Estrogen Administration for the Treatment of NASH in Postmenopausal Women

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexFemale
Age45-70
SponsorMassachusetts General Hospital

About this trial

Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States. Despite this, the treatment options remain limited. Preclinical and preliminary clinical data suggest that estrogen deficiency plays an important role in the pathology of steatosis, inflammation and fibrosis in non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Post-menopausal women are a growing population with particularly high risk of NASH due to their lack of estrogen. This study will examine the effect of estradiol on hepatic fibrosis and fat in post-menopausal women with NASH.

Eligibility criteria

Qualifiers

Postmenopausal women 45-70 years old

NASH by biopsy or NAFLD by imaging within 6 months of screen

Hepatitis C antibody and hepatitis B surface antigen negative

Negative mammogram within 1 year

Disqualifiers

Heavy alcohol use

Use of NASH pharmacotherapies within 12 months of study entry

Known cirrhosis, stage 4 fibrosis on biopsy, or clinical evidence of cirrhosis or portal hypertension on imaging or exam

Participation in NASH clinical trial within 6 months of study entry

Trial design

Treatments tested in this trial

  • Estradiol patch
  • Placebo

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators