Skip to content

Pair antiplatelet therapy for acute ischemic stroke with intracranial artery stenosis

Pair antiplatelet therapy for acute ischemic stroke with intracranial artery stenosis - PATH-ICAS

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066981
Enrollment
Unknown
Registered
2022-12-22
Start date
2023-01-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

ischemic stroke

Interventions

Test Group:Clopidogrel 75mg/day for 90 days
Aspirin 100mg/day for 90 days
Control Group:Clopidogrel 75 mg/day for 30 consecutive days
Aspirin 100 mg/day for 90 consecutive days

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 40 to 75 years old; 2. In line with the WHO definition of stroke, patients with non-cardiac cerebral infarction, those with hemorrhagic cerebral infarction were excluded by head CT/MRI and confirmed as cerebral infarction, and intracranial arterial stenosis was >50% confirmed by MRA/CTA/DSA (intracrnial internal carotid artery, major branches of middle cerebral artery (M1, M2 proximal segment), anterior cerebral artery (A1 segment), posterior cerebral artery (P1 segment), intracranial vertebral artery and basilar artery); 3. The onset of the first stroke is less than 7 days; 4. NIHSS score = 3 points; 5. The patient or family members signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients receiving thrombolysis and thrombectomy; 2. Patients with a history of recurrent stroke; 3. Patients with major surgery or severe trauma in the previous 30 days; 4. history of gastrointestinal bleeding, active peptic ulcer, intracranial hemorrhage, other bleeding diseases 5.contraindication or intolerance of antiplatelet agents 6. platelet count & Lt 100 * 10 ^ 9/L, hemoglobin & LT; 110 g/L; 7. The patients with severe heart, lung, liver and kidney insufficiency and serious combined diseases (for example, severe heart and lung failure, advanced tumor, severe dementia) 8.The patients with poor compliance can not cooperate with the demands of the study.

Design outcomes

Primary

MeasureTime frame
3-month major ischemic events and major bleeding events, including death from cardiovascular and cerebrovascular disease, myocardial infarction, stroke (including ischemic and hemorrhagic), emergency intervention and bleeding academic research alliance criteria (BARC) grade 2 or higher bleeding .;

Secondary

MeasureTime frame
Separate major ischemic events (including myocardial infarction + cerebral infarction), myocardial infarction, cerebral infarction, major bleeding event, disability (mRS>2), cardiovascular and cerebrovascular death or death.;

Countries

China

Contacts

Public ContactNengwei Yu, JieYang, Fuqiang Guo

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

yangjie1126@163.com13678130516

Outcome results

None listed

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