Loading-dose dual antiplatelet therapy for early motor deterioration in minor stroke: a randomized controlled trial

OBJECTIVE: To determine whether loading-dose dual antiplatelet therapy (DAPT) reduces early motor deterioration in supratentorial non-cardioembolic ischemic stroke with motor deficits. METHOD: This single-center, parallel-group randomized controlled trial was conducted in Japan from 1 July 2023, to 30 June 2025. Patients aged 20-85 years presenting within 48 hours of onset with supratentorial non-cardioembolic ischemic stroke, unilateral motor deficit, and no ≥ 50% stenosis or proximal large artery occlusion were randomized 1:1 to loading-dose DAPT or non-loading antiplatelet therapy. The primary outcome was motor deterioration within 7 days, defined as an increase of ≥1 point in the affected-side National Institutes of Health Stroke Scale limb motor subscore. Risk ratios (RRs) and 95% confidence intervals (CIs) were estimated using modified Poisson regression. RESULTS: Of 189 randomized patients, 188 were included in the primary analysis. Motor deterioration occurred in 15/98 patients (15%) in the loading-dose DAPT group and 32/90 (36%) in the non-loading group (RR 0.43; 95% CI, 0.25-0.74). Favorable functional outcomes were more frequent with loading-dose DAPT at day 21 (76% vs 61%; RR 1.24; 95% CI, 1.01-1.51) and day 90 (90% vs 73%; RR 1.23; 95% CI, 1.06-1.42). One intracerebral hemorrhage requiring surgery and one fatal pulmonary hemorrhage occurred in the loading-dose group. CONCLUSION: Loading-dose DAPT initiated within 48 hours was associated with reduced early motor deterioration and better functional outcomes, but larger multicenter trials are needed to confirm efficacy and safety. Trial registration: UMIN000058468; retrospectively registered.

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Journal
Neurological Research
Published
2026-09-14
DOI
https://doi.org/10.1080/01616412.2026.2733685
Primary Topic
Acute Ischemic Stroke Management
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article
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article

Loading-dose dual antiplatelet therapy for early motor deterioration in minor stroke: a randomized controlled trial

Ryuichi Kuroda, Yasukazu Hijikata, Te-Jin Lee, Tetsuro Kawaguchi et al.
Neurological Research
Acute Ischemic Stroke Management
article

Loading-dose dual antiplatelet therapy for early motor deterioration in minor stroke: a randomized controlled trial

Ryuichi Kuroda, Yasukazu Hijikata, Te-Jin Lee, Tetsuro Kawaguchi, Hiroshi Kudo, Naoya Takeda, Eiji Kurihara, Takayuki NAKASHO, Ryosuke IKEO, Takashi Mizowaki, Satoshi Inoue
article en

Abstract

OBJECTIVE: To determine whether loading-dose dual antiplatelet therapy (DAPT) reduces early motor deterioration in supratentorial non-cardioembolic ischemic stroke with motor deficits. METHOD: This single-center, parallel-group randomized controlled trial was conducted in Japan from 1 July 2023, to 30 June 2025. Patients aged 20-85 years presenting within 48 hours of onset with supratentorial non-cardioembolic ischemic stroke, unilateral motor deficit, and no ≥ 50% stenosis or proximal large artery occlusion were randomized 1:1 to loading-dose DAPT or non-loading antiplatelet therapy. The primary outcome was motor deterioration within 7 days, defined as an increase of ≥1 point in the affected-side National Institutes of Health Stroke Scale limb motor subscore. Risk ratios (RRs) and 95% confidence intervals (CIs) were estimated using modified Poisson regression. RESULTS: Of 189 randomized patients, 188 were included in the primary analysis. Motor deterioration occurred in 15/98 patients (15%) in the loading-dose DAPT group and 32/90 (36%) in the non-loading group (RR 0.43; 95% CI, 0.25-0.74). Favorable functional outcomes were more frequent with loading-dose DAPT at day 21 (76% vs 61%; RR 1.24; 95% CI, 1.01-1.51) and day 90 (90% vs 73%; RR 1.23; 95% CI, 1.06-1.42). One intracerebral hemorrhage requiring surgery and one fatal pulmonary hemorrhage occurred in the loading-dose group. CONCLUSION: Loading-dose DAPT initiated within 48 hours was associated with reduced early motor deterioration and better functional outcomes, but larger multicenter trials are needed to confirm efficacy and safety. Trial registration: UMIN000058468; retrospectively registered.

Neurological Research
Kyoto University (JP), Junshin Junior College (JP)
Good health and well-being
Openalex Percentile: Top 11%
Acute Ischemic Stroke Management
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