Safety and Efficacy of Baricitinib After Endovascular Treatment in Acute Anterior Circulation Large Vessel Occlusion: A Multicenter, Randomized Controlled Clinical Trial

Trial statusNot yet recruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorThe First Affiliated Hospital of University of Science and Technology of China

About this trial

The primary purpose of this study is to evaluate the efficacy and safety of Baricitinib combined with endovascular therapy in patients with acute anterior circulation large vessel occlusion, to address futile recanalization with priority, and to elucidating the mechanism of JAK/STAT pathway inhibition on neuroprotection and inflammatory regulation.

Eligibility criteria

Qualifiers

Age is 18 years old or above.

Diagnosed as anterior circulation large vessel occlusion stroke by CTA, MRA or DSA.

Randomized within 24h after the onset.

The NIHSS score is above 5 and the ASPECT score is above 3 points while receiving imaging examination;

Disqualifiers

Intracranial hemorrhage confirmed by CT or MRI.

mRS score>2 for patients <80 years, or mRS score>1 for those ≥80 years before onset.

Pregnant or lactating women.

Allergic to contrast agents.

Trial design

Treatments tested in this trial

  • 2mg Baricitinib
  • 4mg Baricitinib
  • Placebo
  • Guideline-based therapy

Treatment groups

750 Participants
are divided into 3 treatment groups