Skip to main content
Clinical Trials/KCT0009043
KCT0009043Not yet recruitingUnknown

Optimal target LDL level for small vessel occlusion stroke: A multi-center, prospective, randomized, open-label, blinded endpoint trial (SVO70)

Seoul National University Hospital0 sites4,016 target enrollmentStarted: TBDLast updated:
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

Similar Trials

Optimal target LDL level for small vessel... | Clinical Trial