Intensive Rosuvastatin Therapy on Cerebral Hemodynamics in Patients With Atherosclerotic Intracranial Arterial Stenosis
Primary Purpose
Atherosclerosis
Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Rosuvastatin
Sponsored by
About this trial
This is an interventional treatment trial for Atherosclerosis focused on measuring Atherosclerotic Intracranial Arterial Stenosis, Intensive Rosuvastatin Therapy, Computed Tomography Perfusion (CTP)
Eligibility Criteria
Inclusion Criteria:
- Provision of informed consent
- Male and female adults aged 18-80years old
- Recent (within 3 months) ischemic stroke or TIA;
- Intracranial large artery (intracranial internal artery, middle cerebral artery M1, vertebral artery and basilar artery) stenosis between 50-99%.
- Statin naïve:defined as receiving no statin therapy within 3 months
Exclusion Criteria:
- Cardioembolic stroke;
- Rosuvastatin use is contraindicated;
- Allergic to contrast agents;
- Chronic devastating illness, multiple organ failure;
- Dementia or mental disorder unable to return for repeat brain CTP.
- Administration of lipid-lowering drugs (statin, clofibrate, probucol or analog, nicotinic acid, or other prohibited drug) before enrollment.
- Active liver disease or aminopherase ≧3 ULN(Upper Limit of Normal)
- Renal function damage. GFR(Glomerular Filtration Rate) ﹤30ml/min
Sites / Locations
- The second affiliated hospital of Zhejiang University
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
standard dose
intensive dose
Arm Description
Drug: Rosuvastatin rosuvastatin 10 mg daily for 52 weeks.
Drug: Rosuvastatin rosuvastatin 20 mg daily for 52 weeks.
Outcomes
Primary Outcome Measures
the change of relative cerebral blood flow (CBF) (ml/100g/min)by CTP
Secondary Outcome Measures
the changes of relative cerebral blood volume (CBV)(ml/100g) by CTP
the changes of relative mean transit time (MTT)(min) by CTP
the changes of lipid parameters (LDL-C,mmol/L;HDL-C,mmol/L;TG,mmol/L;TC,mmol/L;Apo A,mmol/L;Apo B,mmol/L )
myopathic events, hepatic function, renal function and other adverse events.
Full Information
NCT ID
NCT02594800
First Posted
October 30, 2015
Last Updated
March 29, 2020
Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
1. Study Identification
Unique Protocol Identification Number
NCT02594800
Brief Title
Intensive Rosuvastatin Therapy on Cerebral Hemodynamics in Patients With Atherosclerotic Intracranial Arterial Stenosis
Official Title
The Impact of Intensive Rosuvastatin Therapy on Cerebral Hemodynamics in Patients With Atherosclerotic Intracranial Arterial Stenosis Evaluated by Computed Tomography Perfusion (CTP)
Study Type
Interventional
2. Study Status
Record Verification Date
June 2019
Overall Recruitment Status
Completed
Study Start Date
December 21, 2015 (Actual)
Primary Completion Date
July 12, 2018 (Actual)
Study Completion Date
June 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Second Affiliated Hospital, School of Medicine, Zhejiang University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Atherosclerotic intracranial arterial stenosis (AICAS) corresponds to luminal narrowing of the major intracranial arteries. The prevalence of intracranial atherosclerotic stenosis accounts for 33% to 67% of stroke or transient ischemic attack (TIA) cases in China and other countries in Asia. AICAS is also highly associated with the risk of stroke recurrence. Possible mechanisms of cerebral infarction secondary to AICAS are likely linked with hemodynamic compromise distal to site of stenosis.
Computed tomography perfusion (CTP) can be used to evaluate vasoreactivity and cerebrovascular reserve in patients with AICAS and predict future stroke. The parameters of CTP include ①cerebral blood flow(CBF),② cerebral blood volume(CBV) and ③mean transit time(MTT). Relative regional cerebral blood flow (rCBF) was evaluated as the percentage radioisotope counts in the region of interest (ROI) of the affected side against the corresponding ROI in the unaffected contralateral side.
Statins can decrease the incidence of transient ischemic attack or ischemic stroke and improve stroke outcome. Few studies focus on the relationship between statins therapy and cerebral perfusion.
Whether intensive rosuvastatin therapy compared with standard rosuvastatin therapy can improve hemodynamic situation and cerebral perfusion status in AICAS has not been illustrated.
Based on those studies, the investigators hypothesized that intensive rosuvastatin may also improve the symptoms of AICAS not only through enhancing the stability of atherosclerotic plaques, but also its pleiotropic effects. So it can change the hemodynamic status around the plaque and increase cerebral flow in the downstream territory. So in this study the investigators try to analysis statin's impact on the hemodynamic changes as well as the downstream perfusion which is determined by CTP.
Detailed Description
This is an prospective, randomized, single-blind, single center clinical trial to evaluate the effect of intensive rosuvastatin therapy compared with standard rosuvastatin therapy on improve the cerebral perfusion in Chinese patients with atherosclerotic intracranial arterial stenosis between 50-99%.
The study will enroll 44 patients and randomly divided into 2 groups: standard dose rosuvastatin therapy (SRT 10mg/day)and intensive dose rosuvastatin therapy (IRT 20mg/day)in a 1:1 ratio. Both groups will be prescribed with statin based on other routine medication for stroke for 52 weeks. CTP will be performed at baseline and 52 weeks after treatment. Lipid levels and biochemical examinations will be obtained at baseline and 13, 26, 39, 52 week. AEs(Adverse Events)/SAEs(Serious Adverse Events) will be collected and recorded in CRF(Case Report Form) from the signing of informed consent throughout the study until and including the last visit.
Study Endpoints: Primary endpoint: Compared with standard dose rosuvastatin therapy 10mg/day, the change of relative cerebral blood flow (CBF) by CTP after intensive dose rosuvastatin therapy 20mg/day treatment for 52 weeks.Secondary endpoints: (1) Compared with standard dose rosuvastatin therapy 10mg/day, the changes of relative cerebral blood volume (CBV) by CTP after rosuvastatin 20mg/d treatment for 52 weeks (2) Compared with standard dose rosuvastatin therapy 10mg/day, the changes of relative mean transit time (MTT) by CTP after rosuvastatin 20mg/d treatment for 52 weeks (3) Compared with standard dose rosuvastatin therapy 10mg/day, the changes of lipid parameters (LDL-C, HDL-C, TG(Triglyceride), TC(Total Cholesterol), Apo A and Apo B ) after rosuvastatin 20mg/d for 52 weeks (4) Safety.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atherosclerosis
Keywords
Atherosclerotic Intracranial Arterial Stenosis, Intensive Rosuvastatin Therapy, Computed Tomography Perfusion (CTP)
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)
8. Arms, Groups, and Interventions
Arm Title
standard dose
Arm Type
Active Comparator
Arm Description
Drug: Rosuvastatin rosuvastatin 10 mg daily for 52 weeks.
Arm Title
intensive dose
Arm Type
Experimental
Arm Description
Drug: Rosuvastatin rosuvastatin 20 mg daily for 52 weeks.
Intervention Type
Drug
Intervention Name(s)
Rosuvastatin
Other Intervention Name(s)
Crestor
Intervention Description
standard or intensive dose rosuvastatin therapy based on other routine medication for stroke for 52 weeks.
Primary Outcome Measure Information:
Title
the change of relative cerebral blood flow (CBF) (ml/100g/min)by CTP
Time Frame
52 weeks
Secondary Outcome Measure Information:
Title
the changes of relative cerebral blood volume (CBV)(ml/100g) by CTP
Time Frame
52 weeks
Title
the changes of relative mean transit time (MTT)(min) by CTP
Time Frame
52 weeks
Title
the changes of lipid parameters (LDL-C,mmol/L;HDL-C,mmol/L;TG,mmol/L;TC,mmol/L;Apo A,mmol/L;Apo B,mmol/L )
Time Frame
13, 26, 39, 52 week
Title
myopathic events, hepatic function, renal function and other adverse events.
Time Frame
52 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Provision of informed consent
Male and female adults aged 18-80years old
Recent (within 3 months) ischemic stroke or TIA;
Intracranial large artery (intracranial internal artery, middle cerebral artery M1, vertebral artery and basilar artery) stenosis between 50-99%.
Statin naïve:defined as receiving no statin therapy within 3 months
Exclusion Criteria:
Cardioembolic stroke;
Rosuvastatin use is contraindicated;
Allergic to contrast agents;
Chronic devastating illness, multiple organ failure;
Dementia or mental disorder unable to return for repeat brain CTP.
Administration of lipid-lowering drugs (statin, clofibrate, probucol or analog, nicotinic acid, or other prohibited drug) before enrollment.
Active liver disease or aminopherase ≧3 ULN(Upper Limit of Normal)
Renal function damage. GFR(Glomerular Filtration Rate) ﹤30ml/min
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Min Lou, Ph.D
Organizational Affiliation
Zhejiang University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The second affiliated hospital of Zhejiang University
City
Hangzhou
State/Province
Zhejiang
ZIP/Postal Code
310000
Country
China
12. IPD Sharing Statement
Learn more about this trial
Intensive Rosuvastatin Therapy on Cerebral Hemodynamics in Patients With Atherosclerotic Intracranial Arterial Stenosis
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