KCT0009043Not yet recruitingUnknown
Optimal target LDL level for small vessel occlusion stroke: A multi-center, prospective, randomized, open-label, blinded endpoint trial (SVO70)
Conditions
Trial Snapshot
- Phase
- Unknown
- Status
- Not yet recruiting
- Enrollment
- 4,016
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 19(Year) to o Limit (—)
- Sex
- All
Inclusion Criteria
- •1) Adults aged =19 years
- •2) Patients with small vessel occlusion stroke lesions that can be objectively identified by imaging
- •*small vessel occlusion stroke lesions:
- •The term is defined as the lesions of subcortical cerebral infarction or brainstem cerebral infarction, which can be identified in MRI images or CT (Computed Tomography) images, with a maximum diameter of =15 mm, and it belongs to the area where ischemic stroke due to small vessel occlusion can occur.
- •3) Patients with a history of symptomatic ischemic stroke caused by 2) lesions within 14 days of recruitment
- •4) Patients who voluntarily provide written consent after receiving an explanation of the study
Exclusion Criteria
- •1) Patients whose ischemic stroke is likely to have occurred due to a cause other than small vessel occlusion
- •2) Patients with other medical conditions requiring LDL cholesterol management, and if the treatment guidelines for that condition specify LDL cholesterol control goals.
- •3) Patients who fall under the contraindications or precautions for statin therapy: those with active liver disease, serum transaminase levels elevated more than three times the normal range, neuromuscular disorders, hypersensitivity reactions to medications, or concurrent use of contraindicated drugs, etc.
- •4) Patients who are pregnant or breastfeeding, or who are expecting to become pregnant during the study period
- •5) Patients who are ineligible to continue participating in the trial for at least 2 years, based on the appraisal of at least one investigator
Investigators
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