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Argatroban, aspirin and clopidgrel combination therapy for non-cardioembolic acute ischemic stroke -a prospective, randomized, argatroban and aspirin-controlled study-

Argatroban, aspirin and clopidgrel combination therapy for non-cardioembolic acute ischemic stroke -a prospective, randomized, argatroban and aspirin-controlled study- - Dual antiplatelet therapy for non-cardioembolic acute ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014405
Enrollment
50
Registered
2014-06-27
Start date
2013-12-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Acute non-cardioembolic stroke

Interventions

Dual antiplatelet group: argatoroban, aspirin 100mg (day1 200mg), cropidogrel 75mg(day1 300mg) for 7 days, after day 7 mono antiplatelet agent Mono antiplatelet group: argatroban, aspirin 100mg (da

Sponsors

Department of Neurology Okazaki City Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. non-cardioembolic stroke within 48 hours of onset 2. small vessel disease (lacunar or BAD (branch atheromatous disease)) 3. NIHSS score below 20 points on admission 4. mRS score 0-2 before onset 5. patients written informed consent

Exclusion criteria

Exclusion criteria: 1. cardioembolic stroke 2. antithrombotic therapy (cilostazol, ticlopidine, aspirin 100mg over, clopidogrel 75mg over, anticoagulants) before onset 3. congestive heart failure 4. medical history of allergies of argatroban, aspirin, clopidogrel 5. blood pressure cannot be controlled below 180/105mmHg 6. high hemorrhagic risk 7. severe stenosis of major cerebral and cervical artery 8. patients who are not appropriate to participate in this trial

Design outcomes

Primary

MeasureTime frame
1. NIHSS score at 7 days after admission and at day of discharge 2. modified Rankin scale score at 3 months after stroke

Secondary

MeasureTime frame
1. outcome at hospital discharge 2. TIA, stroke recurrence, intracranial hemorrhage, cardiovascular event within 3 months after stroke

Countries

Japan

Contacts

Public ContactRyoji Nishi

Okazaki City Hospital Department of Neurology

nishi-r@gc4.so-net.ne.jp0564-21-8111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026