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Natural Soybean-derived Femarelle ®for Patients With Non Alcoholic Fatty Liver Disease

Sponsor
Hadassah Medical Organization (Other)
Overall Status
Withdrawn
CT.gov ID
NCT01269320
Collaborator
(none)
0
Enrollment
1
Location

Study Details

Study Description

Brief Summary

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
Phase 4

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Study Start Date :
Jan 1, 2012

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:

    1. Biopsy proven NASH

    2. If suffering from diabetes may be treated by up to 2 oral medications, with stable doses for 2 months.

    3. If participating in sexual activity that could lead to pregnancy, the study volunteer must agree that two reliable methods of contraception will be used simultaneously while receiving the protocol-specified medication and for 1 month after stopping the medication.

    NOTE: Hormonal-based methods alone are not sufficient. At least two of the following methods MUST be used appropriately unless documentation of menopause, sterilization, or azoospermia is present:

    • Condoms (male or female) with or without a spermicidal agent. - Condoms are recommended because their appropriate use is the only contraception method effective for preventing HIV transmission

    • Diaphragm or cervical cap with spermicide

    • IUD

    • Hormonal-based contraception

    Study subjects who are not of reproductive potential (girls who have not reached menarche or women who have been post-menopausal for at least 24 consecutive months or have undergone hysterectomy and/or bilateral oophorectomy are eligible without requiring the use of contraceptives. Written or oral documentation communicated by clinician or clinician's staff is required by one of the following:

    • Physician report/letter

    • Operative report or other source documentation in the patient record (a laboratory report of azoospermia is required to document successful vasectomy)

    • Discharge summary

    • Laboratory report of azoospermia

    • FSH measurement elevated into the menopausal range as established by the reporting laboratory.

    1. Ability and willingness of subject or legal guardian/representative to provide informed consent.
    Exclusion Criteria:

    1. Pregnancy or Breast-Feeding

    2. Continuous use of the following medications for more than 3 days within 30 days of study entry:

    • Immunosuppressives

    • Immune modulators

    • Systemic glucocorticoids

    • Anti-neoplastic agents

    1. Active drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements.

    2. Serious illness requiring systemic treatment and/or hospitalization within 30 days prior to entry.

    3. Surgery within the previous 3 months.

    4. Any serious infectious, cardiac, pulmonary, or kidney disease

    5. Hypersensitivity to Femarelle ®

    6. Malignancy of the uterus or breast

    7. Past thromboembolic event

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Hadassah Medical Organization, Jerusalem, Israel Jerusalem Israel 91120

    Sponsors and Collaborators

    • Hadassah Medical Organization

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01269320
    Other Study ID Numbers:
    • 0172-10-HMO-CTIL
    First Posted:
    Jan 4, 2011
    Last Update Posted:
    Aug 28, 2012
    Last Verified:
    Aug 1, 2011

    Study Results

    No Results Posted as of Aug 28, 2012