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Early Aggressive Strategy for Treatment of Lipid-Lowering in Acute Ischemic Stroke Delivered With Endovascular Therapy for Large Artery Occlusion

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

EAST-LDL is a prospective, multicenter, randomized, open-label clinical trial with blinded endpoint assessment evaluating whether early intensive lipid lowering with the PCSK9 inhibitor recaticimab, administered before endovascular therapy, improves functional outcome in patients with acute ischemic stroke due to anterior-circulation large-vessel occlusion. Participants are randomized to recaticimab plus guideline-recommended standard of care or standard of care alone. The primary outcome is favorable functional outcome, defined as a modified Rankin Scale score of 0-2 at 90 ± 7 days.

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

• Adults (age 18 years and older);

• Imaging diagnosis of acute ischemic stroke with anterior circulation large vessel occlusion (including: internal carotid artery, middle cerebral artery M1 and M2, anterior cerebral artery A1 and A2);

• Planned to undergo endovascular intervention within 24 hours of symptom onset (or last known well time) according to local guidelines;

• Provision of informed consent by the patient or his/her legally authorized representative (or by an appropriate agent according to local requirements).

Locations
Other Locations
China
Shanghai East Hospital, Tongji University
RECRUITING
Shanghai
Contact Information
Primary
Gang Li, MD
ligang@tongji.edu.cn
86021-38804518
Time Frame
Start Date: 2025-06-19
Estimated Completion Date: 2027-06-01
Participants
Target number of participants: 978
Treatments
Active_comparator: Control Group
Guideline-recommended standard of care
Experimental: Investigational Group
Guideline-recommended standard of care+intensive lipid-lowering therapy
Related Therapeutic Areas
Sponsors
Leads: Shanghai East Hospital

This content was sourced from clinicaltrials.gov