Methylprednisolone as Adjunct to Endovascular Thrombectomy for Acute Ischemic Stroke With Large Infarct Core and Post-stroke Lymphocytopenia -A Multicenter, Randomized, Double-blind, Placebo-controlled, Non-inferiority Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The efficacy and safety of early adjunctive methylprednisolone therapy in acute ischemic stroke patients with large infarct cores (ASPECTS score \< 6) and post-stroke lymphocytopenia remain unclear. These immunocompromised patients face higher mortality rates and poorer clinical outcomes, with limited effective treatment options currently available. This multicenter, randomized, double-blind, placebo-controlled, non-inferiority trial aims to demonstrate that early methylprednisolone administration combined with reperfusion therapy is non-inferior to placebo in terms of survival and functional outcomes at 90 days.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years.

• The time from last known well to randomization was within 24 hours.

• Anterior circulation ischemic stroke was preliminarily determined according to clinical symptoms or imaging examination.

• Occlusion of the intracranial internal carotid artery, the M1- or M2-segment of the middle cerebral artery by confirmed by CT angiography (CTA), MR angiography (MRA), or digital subtraction angiography (DSA).

• Baseline National Institutes of Health Stroke Scale (NIHSS) ≥ 6.

• Baseline Alberta Stroke Program Early CT Score (ASPECTS) \< 6 (based on non-contrast CT or MRI) or core infarct volume ≥ 50 ml (based on CTP with rCBF \< 30%).

• Planned treatment with endovascular thrombectomy (EVT).

• Baseline peripheral blood lymphocyte \< 0.8×10#/L

• Informed consent obtained from patients or their legal representatives.

Locations
Other Locations
China
Department of Neurology, the First Affiliated Hospital Fujian Medical University
RECRUITING
Fuzhou
Contact Information
Primary
Yi Lin, MD
linyi7811@163.com
86-13615039153
Backup
Ying Fu, MD
fuying1995@163.com
86-13920263588
Time Frame
Start Date: 2025-09-01
Estimated Completion Date: 2027-09-30
Participants
Target number of participants: 200
Treatments
Experimental: Methylprednisolone sodium succinate group
Placebo_comparator: Methylprednisolone sodium succinate simulant (normal saline placebo)
Related Therapeutic Areas
Sponsors
Leads: YiLin

This content was sourced from clinicaltrials.gov