Study on Rosuvastatin+Ezetimibe and Rosuvastatin for LDL-C Goal in Patients With Recent Ischemic Stroke

NCT03993236 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 584

Last updated 2024-10-03

No results posted yet for this study

Summary

A randomized clinical trial for the comparison of the efficacy and safety of moderate-intensity rosuvastatin plus ezetimibe versus high-intensity rosuvastatin for target LDL-C goal achievement in patients with recent ischemic stroke

Conditions

  • Stroke, Ischemic

Interventions

DRUG

Experimental: Rosuvastatin/Ezetimibe 10

* Rosuvastatin/Ezetimibe 10/10mg * orally administered once daily for 90 days

DRUG

Active Comparator: Rosuvastatin 20mg

* Rosuvastatin 20mg * orally administered once daily for 90 days

Sponsors & Collaborators

  • Ewha Womans University Seoul Hospital

    collaborator OTHER
  • Severance Hospital

    collaborator OTHER
  • Korea University Ansan Hospital

    collaborator OTHER
  • Korea University Guro Hospital

    collaborator OTHER
  • Myongji Hospital

    collaborator OTHER
  • Seoul St. Mary's Hospital

    collaborator OTHER
  • Samsung Medical Center

    collaborator OTHER
  • Seoul National University Hospital

    collaborator OTHER
  • Chung-Ang University Hosptial, Chung-Ang University College of Medicine

    collaborator OTHER
  • Hallym University Medical Center

    collaborator OTHER
  • Kyunghee University Medical Center

    collaborator OTHER
  • Inje University Ilsan Paik Hospital

    collaborator OTHER
  • Keun-Sik Hong

    lead OTHER

Principal Investigators

  • Keun-Sik Hong, MD., PhD. · Department of Neurology, Inje University Ilsan Paik Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-09-09
Primary Completion
2021-09-27
Completion
2021-09-27

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03993236 on ClinicalTrials.gov