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Clopidogrel Resistance in Stroke Patients From Different Ethnicities

Prospective Study Evaluating Clopidogrel Resistance in Ischemic Stroke Patients From Different Ethnicities

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03806894
Enrollment
300
Registered
2019-01-16
Start date
2019-10-31
Completion date
2020-12-31
Last updated
2019-07-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Clopidogrel, Poor Metabolism of, Ischemic Stroke

Brief summary

Clopidogrel is an anti-platelet agent used to inhibit blood clots. Variation in response to clopidogrel has been reported among different population and may lead to reoccurring ischemic events. The aim of the present study is to evaluate the incidence of clopidogrel resistance in ischemic stroke patients from different ethnicities in Northern Israel and to find different strategies to overcome high platelet reactivity including clopidogrel dose adjustment or the choice of alternative agents. Quantification of platelet aggregation will be determined by vasodilator stimulated phosphoprotein (VASP) assay.

Interventions

DIAGNOSTIC_TESTQuantification of platelet aggregation

Platelet aggregation will be determined by vasodilator-stimulated phosphoprotein (VASP) assay

Sponsors

Ziv Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Ability to provide written informed consent and to be compliant with protocol assessments. 2. Ages 18 and above inclusive 3. Both genders eligible for the study 4. Diagnosis of ischemic cerebrovascular event

Exclusion criteria

1. Pregnant patients will be excluded 2. Ages below 18 3. Patients not able to provide informed consent

Design outcomes

Primary

MeasureTime frame
Rates of clopidogrel resistance assessed among the different ethnicities6 months
Identifying of high-risk subgroups of adverse clinical outcomes6 to 12 months

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026