Skip to content

Development of antiplatelet therapy protocol for coil embolization of intracranial aneurysm

Development of antiplatelet therapy protocol for coil embolization of intracranial aneurysm

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0000804
Enrollment
416
Registered
2013-07-24
Start date
2013-05-27
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Drug : 1. Standard vs modified antiplatelet preparation (1) On admission day, high on-treatment reactivity (HTPR) for antiplatelet drugs is evaluated with platelet function test (VerifyNow
Accumetrics, San Diego, CA). (2) Definition of HTPR - Aspirin resistance: &gt
550 of ARU - Clopidogrel resistance: &gt
213 of PRU (3) Study subject without HTPR (non-resistenace group) Standard preparation (aspirin 100mg and clopidogrel 75mg) is maintained on the day of surgery. (4) Study subject with HTPR a. Random

Sponsors

Seoul National University Bundang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Standard vs modified antiplatelet preparation 1. Patients with intracranial aneurysm who plan to undergo coil embolization 2. Patient aged 20 years and more at the day of enrollment 3. Patient with less than 2 of modified Rankin scale score at the day of enrollment 4. Patient who agrees and writes out a consent form Short vs long-term dual antiplatelet therapy 1. Patients with unruptured aneurysm treated with stent-assisted coiling within 30 days at the day of enrollment 2. Patient aged 20 years or more at the day of enrollment 3. Patient who agrees and writes out a consent form

Exclusion criteria

Exclusion criteria: Standard vs modified antiplatelet preparation 1. Patient with histoy of hypersensitivity of aspirin, clopidogrel, cilostazol, or prasugrel 2. Patient with high possibility of active bleeding such as symptomatic intrcranial hemorrhage or active gastric ulcer 3. Patient with bleeding tendency or coagulopathy 4. Patient with thrombocytopenia (< 100,000/mm3 of platelet count within three months before enrollment) 5. Patient with liver disease (> 100 of AST or ALT within three months before enrollment) 6. Patient with renal disease (> 2mg/dL of serum creatinin within three months before enrollment) 7. Patient using anticoagulants 8. Patients with congestive heart failure or angina unable to be controlled 9. Patients with malignant tumor requiring treatment 10. Pregnant or breast-feeding woman 11. Patient in whom physician decision is disqualificiation Short vs long-term dual antiplatelet therapy 1. Patient with modified Rankin scale score of = 1 2. Patient with any procedural events 3. Patient who received stent-assisted coiling for fusiform or dissected aneurysm 4. Patient with side effects of aspirin or clopidogrel 5. Patient with underlying disease requiring continuous dual antiplatelet therapy over 12 months 6. Patient using anticoagulants 7. Patient with a high risk of stroke including arterial fibrillation, occlusion or stenosis of = 30% in extra- or intracranial artery, moyamoya disease, or arteriovenous malformation 8. Patient with a high possibility of active bleeding such as symptomatic intracranial hemorrhage or active gastric ulcer 9. Patient with bleeding tendency or coagulopathy 10. Patient with thrombocytopenia (< 100,000/mm3 of platelet count within three months before enrollment) 11. Patient with liver disease (> 100 of AST or ALT within 3 months before enrollment) 12. Patient with renal disease (> 2mg/dL of serum creatinine within 3 months before enrollment) 13. Patients with congestive heart failure or angina unable to be controlled 14. Patients in whom regular follow-up is unable 15. Patients with poor medical condition or life expectancy of less than 2 years 16. Pregnant or breast-feeding woman 17. Patient in whom physician decision is disqualification

Design outcomes

Primary

MeasureTime frame
Thromboembolic event

Secondary

MeasureTime frame
Unfavorable outcome;Bleeding event

Countries

Korea, Republic of

Contacts

Public ContactGyojun Hwang

Seoul National University Bundang Hospital

Outcome results

None listed

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