About this trial
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.
Eligibility criteria
Qualifiers
Age ≥18 years;
Pre-stroke mRS score of 0-1;
Time from symptom onset to randomization ≤24 hours, including wake-up stroke or unwitnessed stroke. Symptom onset is defined as the last known well time;
Baseline NIHSS score of 6-25;
Disqualifiers
Acute intracranial hemorrhage on CT or MRI;
Bilateral acute stroke or multiple intracranial large vessel occlusions;
Isolated extracranial internal carotid artery occlusion;
History of pseudomembranous colitis or antibiotic-associated colitis;
Trial design
Treatments tested in this trial
- Minocycline hydrochloride capsule
- Placebo capsules of Minocycline hydrochloride capsules
Treatment groups
Sponsors and collaborators
Xiang Luo
Lead sponsor
Tongji Hospital
Sponsor institution