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The Effect of the Nutraceutical "Hemofix" on the Coagulation System

This study has been withdrawn prior to enrollment.
(The collaborator lost interest in a clinical study.)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01651468
First Posted: July 27, 2012
Last Update Posted: November 28, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
HEMOFIX
Yocheved Grossman
Idan Grossman
Information provided by (Responsible Party):
Hadassah Medical Organization
  Purpose
Hemofix is a herbal formula based on traditional Jewish and far eastern medicine created to assist in wound healing and bleeding arrest. It contains herbs such as Red Clover, Liquorice, Raspberry, Ginger and more. The present study will evaluate the formula on the coagulation system.

Condition Intervention
Von Willebrand Disease Menorrhagia Dietary Supplement: HEMOFIX

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Supportive Care
Official Title: Phase 1 Study of the Nutraceutical "Hemofix" Safety and Effect on the Coagulation System

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Primary Outcome Measures:
  • bleeding and blood test results [ Time Frame: one year ]

Enrollment: 0
Study Start Date: September 2016
Estimated Study Completion Date: December 2023
Estimated Primary Completion Date: January 2020 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: HEMOFIX
3 grams a day
Dietary Supplement: HEMOFIX
unique complex herbal mixture

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 75 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy volunteers and volunteers with a mild bleeding disorder

Exclusion Criteria:

  • people with thrombophilic and cardiovascular complications,
  • people who are treated with anti-coagulants,
  • women taking birth control pills
  • people with a history hypercoagulability
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01651468


Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel
Sponsors and Collaborators
Hadassah Medical Organization
HEMOFIX
Yocheved Grossman
Idan Grossman
Investigators
Principal Investigator: David Varon, Prof HMO
  More Information

Responsible Party: Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT01651468     History of Changes
Other Study ID Numbers: HEMOFIX- HMO-CTIL
First Submitted: July 25, 2012
First Posted: July 27, 2012
Last Update Posted: November 28, 2017
Last Verified: February 2017

Keywords provided by Hadassah Medical Organization:
mild bleeding disorder

Additional relevant MeSH terms:
Menorrhagia
Von Willebrand Diseases
Uterine Hemorrhage
Uterine Diseases
Genital Diseases, Female
Menstruation Disturbances
Pathologic Processes
Blood Coagulation Disorders, Inherited
Blood Coagulation Disorders
Hematologic Diseases
Coagulation Protein Disorders
Blood Platelet Disorders
Hemorrhagic Disorders
Genetic Diseases, Inborn