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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT01651468
Other study ID # HEMOFIX- HMO-CTIL
Secondary ID
Status Withdrawn
Phase N/A
First received July 25, 2012
Last updated November 26, 2017
Start date September 2016
Est. completion date December 2023

Study information

Verified date February 2017
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 2023
Est. primary completion date January 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility 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

Study Design


Intervention

Dietary Supplement:
HEMOFIX
unique complex herbal mixture

Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem

Sponsors (4)

Lead Sponsor Collaborator
Hadassah Medical Organization HEMOFIX, Idan Grossman, Yocheved Grossman

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary bleeding and blood test results one year
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