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Randomized trialNew England Journal of Medicine

Trial of Endovascular Therapy for Mild Stroke with Large-Vessel Occlusion

First online Oct 23, 2026On EM Weekly Oct 28, 2026Discovered Oct 28, 2026AI-generated Not yet human-reviewed

Summary

MILD-MT randomized 304 patients in China with anterior-circulation large-vessel occlusion, NIHSS less than 6, a small infarct core, and substantial perfusion mismatch within 24 hours to thrombectomy plus medical management or medical management alone; 300 were included in the modified intention-to-treat analysis. Excellent 90-day outcome (mRS 0-1) occurred in 69.4% versus 50.0% (OR 2.32, 95% CI 1.41-3.81; P<0.001). Symptomatic intracranial hemorrhage occurred in 3 patients in each group, while serious procedure-related complications occurred in 19 of 144 thrombectomy patients (13.2%).

Why it matters

The trial challenges a default medical-management approach for mild-deficit LVO when perfusion imaging shows substantial tissue at risk. For a highly selected patient with mild symptoms and LVO, early thrombectomy-center consultation is more defensible, but these data do not support indiscriminate EVT for every low-NIHSS LVO.

Study at a glance

Design
Randomized trial
Population
Patients with anterior-circulation large-vessel occlusion ischemic stroke, NIHSS less than 6, small infarct core, and substantial perfusion mismatch within 24 hours.
Sample size
304
Intervention
Endovascular therapy plus medical management.
Comparator
Medical management alone.
Primary endpoint
Excellent functional outcome, defined as modified Rankin scale 0 or 1, at 90 days.

Main findings

  • mRS 0-1 at 90 days occurred in 69.4% with thrombectomy versus 50.0% with medical management alone (OR 2.32, 95% CI 1.41-3.81; P<0.001).
  • Symptomatic intracranial hemorrhage within 48 hours occurred in 3 patients in each group.
  • Serious procedure-related complications occurred in 19 of 144 thrombectomy patients (13.2%).
  • One death occurred among all participants, in the thrombectomy group.

Limitations

The study was open-label, conducted in China, and selected patients using small-core and large-perfusion-mismatch imaging criteria. Serious procedure-related complications occurred in 13.2%, and applicability outside the studied population remains uncertain.

Read the primary source

Full text: Abstract available; full text paywalled.

Original source

DOI: 10.1056/NEJMoa2609149

PMID: 42929671

Source retrieved Oct 28, 2026. Abstract reviewed; full text unavailable. Primary PubMed record and DOI metadata were verified.

Corrections & review history

No corrections recorded. Human review: not yet human-reviewed.