CClinicalTrials.gg
Status unknownNCT01210248Updated Sep 28, 2010

Correlation Between CYP2C19 Genotype, Level Of Clopidogrel Metabolite And Platelet Inhibition Status

An observational study in PRIMARY FOCUS:PATIENT THAT TAKE CLOPIDOGREL, sponsored by Assaf-Harofeh Medical Center. Status unknown at 1 site in Israel. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2010-09-28.

Sponsored by Assaf-Harofeh Medical Center · Observational

The sponsor has not verified this record recently (last verified May 2010), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
500
Ages
18 Years and older
Sex
All
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Study summary

The aim of this study is to check correlation between CYP2C19 genotype level of clopidogrel metabolite in plasma and platelet inhibition status.

Read the 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:

  1. GENETIC (FOR CYP450 2C19)
  2. PLATELET MAPPING TEST ( BY THROMBOELASTOGRAPH ASSAY)
  3. CLOPIDOGREL INACTIVE METABOLITE DETERMINATION BY CHROMATOGRAPHIC METHOD
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Conditions studied

  • PRIMARY FOCUS:PATIENT THAT TAKE CLOPIDOGREL
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In context

Lead sponsor

Assaf-Harofeh Medical Center is the lead sponsor of 258 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

THE RESEARCH WILL INVOLVE PATIENTS THAT TAKE CLOPIDOGREL AND READY TO GIVE INFORMED CONSENT FOR GENETIC TESTING.

Inclusion criteria

  • > 18 OLD PATIENTS
  • THAT TAKE CLOPIDOGREL MORE THAN 1 WEEK

Exclusion criteria

Exclusion Criteria:

  • PREGNANCY
  • CHRONIC LIVER DISEASES
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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
500 participants (estimated)

Interventions

  • OtherBLOOD COLLECTION

    BLOOD SAMPLE WILL BE COLLECTED FOR 3 KINDS OF TESTS

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Study locations

1 of 1 sites recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01210248
Lead sponsor
Assaf-Harofeh Medical Center
First posted
Sep 28, 2010
Start date
Sep 2010
Primary completion
Jan 2012
Last update
Sep 28, 2010

Study contacts

ADINA BAR HAIM, PhD
Contact
dinab@asaf.health.gov.il
08-9779897
VICTORIA PAPIASHVILI, M.Sc
Contact
victoriapapi@yahoo.com
0577345973
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in May 2010. You cannot join it, but the record below documents what was studied.

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