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Randomized controlled clinical study of medium-intensity statins combined with ezetimibe and high-intensity statins for lipid-lowering treatment of acute ischemic cerebrovascular disease

Randomized controlled clinical study of medium-intensity statins combined with ezetimibe and high-intensity statins for lipid-lowering treatment of acute ischemic cerebrovascular disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057789
Enrollment
Unknown
Registered
2022-03-17
Start date
2022-03-07
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute ischemic stroke/transient ischemic attack

Interventions

Group 1:moderate intensity statins with ezetimibe
Group 2:high intensity statins

Sponsors

The Fifth Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years. 2. In the acute period of ischemic stroke, that is, within 1 week after the onset of mild ischemic stroke (NIHSS score =16 points), and within 2 weeks after the onset of other TIA patients and within 1 week after the onset of TIA patients. 3. Patients or family members sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating patients; 2. Cardiogenic TIA or stroke; 3. Ischemic cerebrovascular diseases caused by vascular malformations, tumors, abscesses, revascularization surgeries or trauma and other non-atherosclerotic diseases; 4. Intracranial hemorrhage; 5. Known allergy to statins or ezetimibe; 6. Active liver disease or liver dysfunction, defined as >=2 times the upper limit of normal (ULN) for aspartate aminotransferase (AST) or alanine aminotransferase (ALT); 7. Blood diseases that may lead to thrombosis; 8. Endarterectomy was performed within 1 month; 9. Severe renal insufficiency or nephrotic syndrome; 10. Serum creatine kinase >=5 times the upper limit of normal (ULN); 11. Participate in another clinical study within 30 days; 12. Any disease or abnormality that the investigator believes may endanger the patient's safety during the study period; 13. Patients who have used any medication known to affect lipid levels or immunosuppressants, azole antifungals or drugs that can cause rhabdomyolysis when used in combination with statins within the last 1 month, or probucol within 6 months.

Design outcomes

Primary

MeasureTime frame
Low density lipoprotein cholesterol levels meet the standard rate;

Countries

China

Contacts

Public ContactZhang Lei

The Fifth Affiliated Hospital of Sun Yat-sen University

zhangl92@sysu.edu.cn+86 13726209240

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026