Skip to content

Pharmacogenetic analysis of Clopidogrel metabolism in coil embolization assisted by stent for cerebral aneurysms

Pharmacogenetic analysis of Clopidogrel metabolism in coil embolization assisted by stent for cerebral aneurysms: Evaluation of clinical safety and efficacy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009849
Enrollment
200
Registered
2024-10-16
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-11-14

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

Conditions

None listed

Interventions

Genetic : The pre-procedure assessment of patients, who have provided informed consent for the clinical trial, includes evaluating their condition. In addition to the ARU and PRU tests, which are clin
if immediate transport is not possible, the sample should be refrigerated until testing. DNA sequencing is performed according to the diagnostic guidelines of the hospital's Department of Laboratory M

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Adult women and men aged 19 to under 75 years - Individuals planning to undergo stent-assisted coil embolization for unruptured cerebral aneurysms who are taking antiplatelet agents before the procedure and have undergone platelet function testing - Modified Rankin Scale (mRS) score = 2 at screening - Individuals who have received a full explanation of the study and have provided final consent to participate

Exclusion criteria

Exclusion criteria: - Individuals with neurological deficits at the time of aneurysm treatment (modified Rankin Scale score of 3 or higher) making it impossible to assess complications - Individuals with known allergic reactions to aspirin or clopidogrel - Individuals at high risk of excessive bleeding due to conditions such as intracranial hemorrhage or severe gastric ulcers - Individuals with a bleeding tendency or coagulation disorders - Individuals deemed at high risk for embolic stroke by the investigator, such as those with atrial fibrillation requiring dual antiplatelet or anticoagulant therapy, extracranial or intracranial vessel occlusion or stenosis greater than 70%, moyamoya disease, or cerebrovascular malformations - Individuals with other intracranial conditions (e.g., brain tumors, moyamoya disease, cerebrovascular malformations) - Individuals with uncontrolled heart failure or angina - Individuals with malignant tumors requiring treatment - Pregnant women, women who might be pregnant, and breastfeeding women - Individuals who are unconscious at the time of diagnosis - Individuals with thrombocytopenia ( 100 IU/L) - Individuals with renal disease (creatinine > 2 mg/dL or eGFR < 30 ml/min/1.73m²) - Individuals unable to comply with regular follow-up - Individuals with poor medication adherence for various reasons - Individuals with psychiatric disorders - Individuals with a medical condition indicating a life expectancy of less than two years - Any other individuals deemed unsuitable for clinical trial participation by the investigator

Design outcomes

Primary

MeasureTime frame
CYP2C19 DNA sequencing

Secondary

MeasureTime frame
ARU(Aspirin Response Unit), PRU(P2Y12 Reaction Unit)

Countries

Korea, Republic of

Contacts

Public ContactMinwoo Kim

Asan Medical Center

surmw0317@naver.com+82-2-3010-1710

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026