- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01210248
Correlation Between CYP2C19 Genotype, Level Of Clopidogrel Metabolite And Platelet Inhibition Status
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
THE FIRST PHASE OF THE RESEARCH WILL INVOLVE PATIENTS RECRUITMENT AND INFORMED CONSENT FOR GENETIC TESTING.THE MAJORITY OF PATIENTS WILL BE RECRUITED FROM EMERGENCY DEPARTMENT. EVERY PATIENT WILL BE ASKED ABOUT HIS AND HIS PARENT'S ETHNICITY (ASHKENASI OR SEPHARDY JEW) AND ADDITIONAL DRUGS HE TAKES. IF PATIENT AGREES TO PARTICIPATE IN THE STUDY , HIS BLOOD SAMPLE WILL BE COLLECTED FOR 3 KINDS OF TESTS:
- GENETIC (FOR CYP450 2C19)
- PLATELET MAPPING TEST ( BY THROMBOELASTOGRAPH ASSAY)
- CLOPIDOGREL INACTIVE METABOLITE DETERMINATION BY CHROMATOGRAPHIC METHOD
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: ADINA BAR HAIM, PhD
- Phone Number: 08-9779897
- Email: dinab@asaf.health.gov.il
Study Contact Backup
- Name: VICTORIA PAPIASHVILI, M.Sc
- Phone Number: 0577345973
- Email: victoriapapi@yahoo.com
Study Locations
-
-
-
Zeriffin, Israel
- Recruiting
- Assaf Harofeh Medical Center
-
Contact:
- ADINA BAR HAIM, PhD
- Phone Number: 08-9779897
- Email: dinab@asaf.health.gov.il
-
Contact:
- VICTORIA PAPIASHVILI, M.Sc
- Email: victoriapapi@yahoo.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- > 18 OLD PATIENTS
- THAT TAKE CLOPIDOGREL MORE THAN 1 WEEK
Exclusion Criteria:
- PREGNANCY
- CHRONIC LIVER DISEASES
Study Plan
How is the study designed?
Design Details
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- NO 51/10
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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