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Completed

NCT Number: NCT04072705

Clopidogrel Preventive Effect Based on CYP2C19 Genotype in Ischemic Stroke

The hypothesis of this study is that "the poor metabolizer or intermediate metabolizer of the cytochrome P450 2C19 genotype in patients with acute ischemic stroke is associated with increased risk of composite cardiovascular events (recurrent stroke, myocardial infarction, cardiovascular death) compared to those who of extensive metabolizer of the cytochrome P450 2C19 genotype".

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Key information

Age range

19 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Yongin Severance Hospital, Yongin-si, Gyeonggi-do, South Korea

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About this study

Clopidogrel, one of the antiplatelet agents used for secondary prevention in patients with ischemic stroke and coronary artery disease, has been shown to have a superior antiplatelet effect compared to aspirin, and is therefore being administered to many patients with stroke and coronary artery disease. Clopidogrel inhibits platelet-derived ADP receptor, P2Y12, in the liver to produce an anti-platelet effect. It has been suggested that clopidogrel resistance could be occurred from drug-drug interaction via the same pharmacological metabolic pathway. Previous studies reported that the genotypes of Cytochrome P450 2C19, which is involved in the metabolism of clopidogrel in the liver, lead to differences in drug response and recurrence rates of cardiovascular disease. The risk of recurrence of ischemic stroke was reported to be about 4 times higher in patients with a poor metabolizer or intermediate metabolizer genotype of the Cytochrome P450 2C19 genotype compared to the extensive metabolizer genotype. This genotypes of Cytochrome P450 2C19 were also different according to race.

The researches about cytochrome P450 2C19 genotype and clopidogrel resistance have been conducted mainly in patients with coronary artery disease and are not known in stroke patients. Few studies have examined whether the resistance of clopidogrel according to the genotype of cytochrome P450 2C19 in stroke patients is related to the occurrence and/or recurrence of cardiovascular disease. The hypothesis of this study is that "the poor metabolizer or intermediate metabolizer of the cytochrome P450 2C19 genotype in patients with acute ischemic stroke is associated with increased risk of cardiovascular disease and mortality compared to those who of extensive metabolizer of the cytochrome P450 2C19 genotype".

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ischemic stroke confirmed by brain CT or MRI
  • Patient who received clopidogrel within 72 hours after onset of ischemic stroke
  • Adults over 19 years
  • Patients who agreed to participate in this study within 7 days after ischemic stroke
  • Patients who underwent Cytochrome P450 2C19 genotype test.

Exclusion criteria

  • Patients who currently take anticoagulation or is expected to take anticoagulation with 6 months from the screening date
  • Patients who need other antiplatelet drugs except aspirin and clopidogrel
  • Patients who were taking clopidogrel prior to ischemic stroke
  • Patients scheduled for coronary artery stenting, coronary artery bypass surgery, carotid endarterectomy, carotid and cerebral artery stenting
  • Patients with severe comorbidities or active cancer with an estimated life expectancy of less than two years
  • Patients who participated in other drug clinical trials within the past 30 days
  • Patients with high risk source of potential cardiac source of embolism in TOAST classification
  • Patients who are expected to unable to participate or continue the study

Treatment and study plan

General principles of care and judgement of researcher

Drug

Because our study will be performed by observational design, there will be no intervention for our study. Because it is a registry-based study, overall decision making for medications will be performed according to the general principles of care and judgement of researcher.

Primary outcomes

  1. composite cardiovascular events

    Time frame: up to 6 months

    Occurrence of composite cardiovascular events (recurrent stroke, myocardial infarction, cardiovascular death)

Secondary outcomes

  1. cardiovascular events

    Time frame: up to 6 months

    Occurrence of ischemic stroke

  2. cardiovascular events

    Time frame: up to 6 months

    Occurrence of transient ischemic attack

  3. cardiovascular events

    Time frame: up to 6 months

    Revascularization of cerebral, coronary, peripheral artery or aorta

  4. cardiovascular events

    Time frame: up to 6 months

    Occurrence of myocardial infarction

  5. early neurological worsening

    Time frame: up to 7 days

    increased National Institutes of Health Stroke Scale within 7 day after admission)

  6. Prognosis

    Time frame: 3 months

    ratio of modified Rankin scale (0 - 2) at 3 months

Other outcomes

  1. Incidence of major adverse events

    Time frame: Tile frame: participants will be followed at 0, 1, 3, 6 months

    Occurrence of major bleeding (fatal bleeding, symptomatic cerebral hemorrhage, ocular hemorrhage, bleeding which needs absolute bed rest or hospitalization or transfusion (more than 2 pack of whole blood or RBC).

    Occurrence of all-causes mortality

Sponsors and collaborators

Lead sponsor

Gangnam Severance Hospital

Other

Collaborators

  • SAMJIN PHARM

Registry information

Official study title

A Multicenter Prospective observationaL Study to evAluate the effecT of Clopidogrel on the prEvention of Major vascuLar Events According to the gEnotype of Cytochrome P450 2C19 in Ischemic Stroke paTients; PLATELET Study

Important dates

Study start
2019
Primary completion
2023
Study completion
2023
First posted
Aug 28, 2019
Registry last updated
Sep 25, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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