Natural Soybean-derived Femarelle ®for Patients With Non Alcoholic Fatty Liver Disease
|ClinicalTrials.gov Identifier: NCT01269320|
Recruitment Status : Withdrawn (Sponsors decision)
First Posted : January 4, 2011
Last Update Posted : August 28, 2012
This is a Single -arm, open-label, before-and after exploratory trial of 90 days of Femarelle ® to improve NAFLD and the metabolic syndrome.
Ingestion of Femarelle will improve non alcoholic steatohepatitis and the metabolic syndrome in patients suffering from these conditions.
Subjects will receive treatment with Femarele 530 mg (1 capsule twice a day) for 90 days and will then be monitored off study treatment for an additional 4 weeks.
|Condition or disease||Intervention/treatment||Phase|
|Nash||Drug: Femarelle||Phase 4|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||0 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Study Start Date :||January 2012|
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01269320
|Hadassah Medical Organization, Jerusalem, Israel|
|Jerusalem, Israel, 91120|