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Recruiting NCT05397405

NCT05397405 Improving Blood Lipid Management in Symptomatic Intracranial Atherosclerotic Stenosis on Clinical Outcome

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Clinical Trial Summary
NCT ID NCT05397405
Status Recruiting
Phase
Sponsor Nanjing First Hospital, Nanjing Medical University
Condition Intracranial Artery Stenosis
Study Type INTERVENTIONAL
Enrollment 180 participants
Start Date 2022-05-23
Primary Completion 2026-05-01

Trial Parameters

Condition Intracranial Artery Stenosis
Sponsor Nanjing First Hospital, Nanjing Medical University
Study Type INTERVENTIONAL
Phase N/A
Enrollment 180
Sex ALL
Min Age 18 Years
Max Age 85 Years
Start Date 2022-05-23
Completion 2026-05-01
Interventions
PCSK9 inhibitor

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Brief Summary

sICASBLM is a prospective controlled trial, to asses the impact of improving blood lipid management on clinical outcome of moderate to severe symptomatic intracranial atherosclerotic stenosis patients (LDL-C\>1.8mmol/L) without endovascular therapy.

Eligibility Criteria

Inclusion Criteria: 1. Age ≥18 years 2. Symptomatic intracranial atherosclerotic stenosis of moderate to severe, did not receive intravenous thrombolysis, thrombectomy, stent implantation and other intravascular treatment 3. low density lipoprotein cholesterol \> 70mg/dl (1.8mmol/L) 4. Receive 3T magnetic resonance angiography or multi-mode MR (high resolution is required), angiography can be included, and images for analysis can be obtained. 5. Lipid-lowering indications of statins 6. Signed an approved informed consents Exclusion Criteria: 1. Contraindications to statins 2. There are contraindications to MRI examination or cannot accept MRI examination 3. Stenosis caused by vasculitis, arterial dissection and moyamoya disease 4. Patients with active bleeding or obvious bleeding tendency 5. Severe heart, lung, renal insufficiency, malignant tumor or other malignant diseases, and death is highly likely within 7 days; pregnancy or women who are lactating 6. Uncontrolled severe diabetes

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