Resuvastatin Treatment for Symptomatic Middle Cerebral Artery Stenosis Based on High-resolution Magnetic Resonance Imaging

NCT ID: NCT02041117

Last Updated: 2020-07-27

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 162 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-02-24
• Study Completion Date: 2018-11-06

Brief Summary

1. It is a multicenter, open-label, sing arm study to evaluate the effects of treatment of Rosuvastatin 10-20mg in volume and morphology of atherosclerotic plague by reducing LDL-C level to or less than 70mg/dl.

2. Ischemic stroke patients will be enrolled within 1 month after stroke onset.

3. Patients will be visited at 0m, 1m, 3m, 6m, 9m, 12m, 18m and 24m.

Conditions

Intracranial Arterial Stenosis

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Rosuvastatin

Group Type: OTHER

Rosuvastatin

Intervention Type: DRUG

Rosuvastatin, 10mg for 4-weeks, then according to the results of the LDL-C, adjust dose of rosuvastatin, maximum to 20 mg/d, to reduce LDL-C under 70 mg/dl for two years.

Interventions

Rosuvastatin

Rosuvastatin, 10mg for 4-weeks, then according to the results of the LDL-C, adjust dose of rosuvastatin, maximum to 20 mg/d, to reduce LDL-C under 70 mg/dl for two years.

Intervention Type: DRUG

Other Intervention Names

Crestor

Eligibility Criteria

Inclusion Criteria

1. Male or female patients between 18 and 75 years of age.

2. Ischemic stroke originate from middle cerebral artery(MCA) AS stenosis, stroke onset within 1 month.

3. LDL-C level is more than 70mg/dl (1.8mmol/L), but less than 250mg/dl (6.5mmol/L); and triglyceride level is less than 353mg/dl (4.0mmol/L).

4. total term of statin therapy less than 2 month in past 1year before entering the study.

（5）30-70% intracranial artery stenosis in M1 segment of MCA comfirmed by CTA or MRI at least 1 or more atherosclerotic plaques in M1 segment of MCA is detectable.

（6）Female patients must agree to use an effective form of birth control throughout the 2-year study treatment period.

（7）The patients who are willing to be enrolled have to remain on the low cholesterol dietary for the study duration.

（8）The patient must be able to comply with scheduled visits, the treatment plan and all laboratory tests.

（9）Written informed consent is provided to participate in the study.

Exclusion Criteria

1. Any hemorrhagic stroke or hemorrhagic infarction

2. Presence of any of cardiac sources of embolism

3. Ischemic stroke caused by non MCA stenosis

4. The patients has LDL cholesterol ≤ 70mg/dl or familial hypercholesterolemia.

5. Previous treatment of target lesion with a stent, angioplasty, or other mechanical device, or plan to perform staged angioplasty within 2 years

6. Any aneurysm proximal to or distal to stenotic intracranial artery

7. Intracranial tumor (except meningioma) or any intracranial vascular malformation

8. Thrombolytic therapy within 24 hours before enrollmentnt

9. The patient has plans for surgical/endovascular intervention for intracranial, carotid, coronary and/or peripheral arterial disease during the course of the study.

10. The patient has or is being treated or evaluated for diagnosed tuberculosis.

11. The patient has a history of malignant neoplasm within the previous 5 years (exception: curable non-melanoma skin malignancies).

12. The patient has a known immunodeficient state (e.g., human immunodeficiency virus) or is being treated with immunosuppressive drugs including cyclosporine.

13. The patient has any other clinically significant medical condition that, in the opinion of the Investigator, could impact the patient's ability to successfully complete the trial.

14. Life expectancy of patients is less than 2 years.

15. The patient have to take medicines as follow: Hormonal therapy, Cyclosporine and other lipid lowering agents: fish oil, garlic essential oil etc.

16. The patient has a history of recent alcohol abuse, drug abuse or significant mental illness.

17. The patient has any condition that would prevent the patient from giving voluntary informed consent.

18. The patient has an inability to tolerate oral medication administration.

19. The patient has a known or suspected allergy to the study medication(s) or the class of study medication to be administered.

20. The patients cannot finish HR-MRI for any reasons.

21. Pregnancy or of childbearing potential and unwilling to use contraception for the duration of this study

22. The patient is enrolled or plans to enroll in another clinical drug or device/interventional trial during this study.

23. The patient has the history of epilepsy/seizures.

24. The patient has liver function tests > 1.5 times the upper limit of normal, serum creatinine > 2.0 mg/dL, GFR < 30 ml/min or has abnormal laboratory values which are deemed clinically significant by the investigator.

25. The patient has the history of myopathy.

26. The patient has thyroid stimulating hormone > 1.5xULN.

27. BMI ≥ 30 kg/m2

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Beijing Tiantan Hospital

OTHER

Sponsor Role: lead

Responsible Party

Yongjun Wang

Executive Vice-President

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Beijing Tiantan Hospital affliated to Capital Medical University

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

2012ZX09303-005-001

Identifier Type: -

Identifier Source: org_study_id