Infarct Growth After Intravenous Tocilizumab in Adults With Acute Ischemic Stroke Undergoing Endovascular Thrombectomy - ILLUMINATE

Study acronym: Illuminate
StatusNot Yet Recruiting
PhasePhase 2/3
Started

Free. We email you which fields changed when ClinicalTrials.gov updates this record.

Track this trial
View on ClinicalTrials.gov ↗

Record History

  1. Minor Study First Submitted
3,537 trials monitored
See 161 trials at risk
The goal of this phase II, placebo-controlled intervention study is to investigate whether tocilizumab, an interleukin-6 (IL-6) receptor inhibitor, may have a neuroprotective effect by reducing infarct growth in adults with acute ischemic stroke. The main question it aims to answer is: Does treatment with tocilizumab given before or during endovascular therapy (EVT) reduce infarct growth 72 hours after EVT compared with placebo in adults with acute ischemic stroke? Researchers will compare tocilizumab with placebo to determine whether infarct growth is smaller in participants receiving tocilizumab. Participants will: Receive either a single dose of tocilizumab or placebo before or during EVT. Undergo standard endovascular treatment for acute ischemic stroke. Undergo brain MRI approximately 72 hours after EVT to assess infarct growth. Have clinical assessments and other study-related examinations and follow-up according to the study protocol.
Trial Details
NCT Number NCT07870681
Lead Sponsor Oslo University Hospital
Collaborators: Copenhagen University Hospital, Rigshospitalet, University Hospital, Akershus, Aarhus University Hospital, Aalborg University Hospital, Odense University Hospital
Conditions
(from sponsor)
Acute Ischemic Stroke
Related terms Ischemic Stroke
Enrollment 156 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov