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Study identifier: NCT07594314 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Minocycline After Successful Endovascular Thrombectomy Recanalization in Acute Anterior Circulation Large Vessel Occlusion (ATTRACTION-MINOA)

Condition: Acute Ischemic Stroke · Vessel Occlusion · Endovascular Thrombectomy  ·  Sponsor: Xiang Luo

PhasePhase 2/Phase 3
Planned participants860
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Endovascular thrombectomy (EVT) improves outcomes in patients with acute large vessel occlusion (LVO). However, despite successful recanalization rates exceeding 80%, fewer than 50% of patients achieve favorable functional outcomes at 90 days, indicating a high rate of futile recanalization. Potential mechanisms include no-reflow, reperfusion injury, and microcirculatory dysfunction, which are closely associated with post-recanalization neuroinflammation. Minocycline is a second-generation tetracycline with pleiotropic neuroprotective effects, including inhibition of microglial activation, reduction of inflammatory mediators, suppression of matrix metalloproteinases, attenuation of oxidative stress, and preservation of blood-brain barrier integrity. Prior preclinical and clinical studies suggest that minocycline may improve neurological outcomes in acute ischemic stroke. This study is a multicenter, prospective, double-blind, randomized controlled trial designed to evaluate the safety and efficacy of adjunctive minocycline in patients with acute anterior circulation LVO who achieve successful recanalization after EVT. The trial will assess whether early administration of minocycline improves functional outcomes and reduces futile recanalization.

This description comes directly from the study's public registry record.

Talk to the study team

Xiang Luo  ·  +86-13349893413  ·  flydottjh@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tongji Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07594314