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This clinical study is designed to evaluate the safety of oral administration of the medical food Hoodia to patients with non alcoholic fatty liver disease. Oral administration of Hoodia is common in many western world countries for appetite suppression and as a food supplement or medical food used for dietary purposes. Nonalcoholic steatohepatitis or NASH is a common, often "silent" liver disease which affects about 2%-5% of Americans. NASH is strongly associated with the metabolic syndrome, diabetes type-2 and obesity and can lead to cirrhosis, HCC, liver transplantation or death.This clinical trial has been designed to assess the safety of short term oral administration of Hoodia to patients with NASH.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
Hadassah Medical Center
Jerusalem, Israel
Start Date
May 1, 2009
Primary Completion Date
June 1, 2010
Completion Date
August 1, 2010
Last Updated
September 17, 2010
20
ESTIMATED participants
Hoodia gordonii
DIETARY_SUPPLEMENT
Placebo
OTHER
Lead Sponsor
Hadassah Medical Organization
NCT06819917
NCT07221227
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06218589