DEB for Symptomatic Intracranial Atherosclerosis Stenosis
Study Details
Study Description
Brief Summary
A prospective, multi-center, single-arm study to evaluate the safety and efficacy of drug eluting balloon catheter for the treatment of patients with symptomatic intracranial atherosclerotic stenosis.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This is a prospective, multi-center, single-arm study to evaluate the safety and efficacy of drug eluting balloon catheter (Vmoky) produced by Yinyi (Liaoning) Biotech Co., Ltd. for the treatment of patients with symptomatic intracranial atherosclerotic stenosis.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Drug eluting balloon (Vmoky) A paclitaxel eluting balloon produced by Yinyi (Liaoning) Biotech Co., Ltd. Balloon length: 8-40 mm, diameter：1.25-5.00 mm. |
Device: Drug eluting balloon (Vmoky)
Use Vmoky Drug Eluting Balloon to treat patients with symptomatic intracranial atherosclerosis stenosis
|
Outcome Measures
Primary Outcome Measures
- Restenosis [6 months (+60 days)]
Restenosis was defined as greater than 50% stenosis within or immediately adjacent (within 5 mm) to the implanted balloon(s) or stent(s) and greater than 20% absolute luminal loss.
Secondary Outcome Measures
- Angiographic success rate [immediately after procedure]
TICI 3 blood flow, residual stenosis no more than 50% after 5 minutes and no flow-limited dissection
- The success rate of device [immediately after procedure]
device successfully cross the lesion and inflate, post-procedural residual stenosis no more than 50%, no use of bail-out stent
- The success rate of procedure [In-hospital (Maximum 7 days after procedure)]
Base on the device success, there is no stroke or death in-hospital
- Target lesion stenosis [6 months (+60 days) and 12 months (±60 days)]
Calculate the stenosis degree with Quantitative Coronary Angiography (QCA) method
- Restenosis [12 months (±60 days)]
Restenosis was defined as greater than 50% stenosis within or immediately adjacent (within 5 mm) to the implanted balloon(s) or stent(s) and greater than 20% absolute luminal loss.
- Stroke events [30 days (±7 days), 6 months (±60 days) and 12 months (±60 days)]
Number of participants that occur these events
- Ischemic stroke and transient ischemic attack (TIA) in the area of the responsible blood vessels [30 days (±7 days), 6 months (±60 days) and 12 months (±60 days)]
Number of participants that occur these events
- Ischemic stroke and transient ischemic attack (TIA) out of the area of the responsible blood vessels [30 days (±7 days), 6 months (±60 days), 12 months (±60 days)]
Number of participants that occur these events
- Non-stroke bleeding [12 months (±60 days)]
Number of participants that occur this event
- Mortality [30 days (±7 days), 6 months (±60 days) and 12 months (±60 days)]
Number of participants that occur this event
- Serious adverse events and adverse events [12 months (±60 days)]
Number of participants that occur these events
Eligibility Criteria
Criteria
Inclusion Criteria:
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Age 18 to 80 years old；
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Symptomatic intracranial artery stenosis, the degree of intracranial diseased artery vascular stenosis measured under cerebral angiography between 70~99% (WASID method)；
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Symptoms are still recurrent after conservative medication (symptoms refer to stroke and transient ischemic episodes of the brain)，or intracranial artery stenosis combined with remote low perfusion performance (rCBF or rCBV abnormalities) in patients.
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The stenotic vessels are located in the internal carotid artery (intracranial segment), middle cerebral artery, vertebral artery (intracranial segment), basilar artery, distal blood vessels are normal；
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Only one lesion needed to be treated；
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The intracranial artery needed to be treated l art mm in diameter；
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Pre-expansion must be satisfied: forward blood flow TICI 3 level, pre-expanded guide wire retention, observation for 5 minutes, residual stenosis is still ≤50%; without blood limited dissection；
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Patients have at least 1 porridge plaque risk factor, including past or existing hypertension, diabetes, hyperlipidemia, smoking;
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mRS≤3 points；
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Patients or their guardians are able to understand the purpose of the trial, voluntarily participate in and sign a written informed consent form, and receive follow-up visits from patients.
Exclusion Criteria:
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Target lesion is in-stent restenosis；
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Exist lesion stenosis more than 50% out of the target vessel；
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Intracranial haemorrhage occurred within 3 months (substantial cerebral hemorrhage, large amount of subcranial hemorrhage, subdural/external bleeding)；
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Acute ischemic stroke has occurred in the last two weeks；
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Stenosis caused by non-atherosclerosis: e.g. arterial mezzanine, moya-moya disease, vasculitis, radioactive vascular disease or fibrous muscle dysplasia;
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Severe calcified, angulate and Mori type C lesions, as well as congenital development of thin blood vessels and fenestration；
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Combine intracranial tumors, aneurysms, or intracranial venous malformations；
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There are risk factors that can lead to cardiogenic embolism: fibrillation, left-ventricle thrombosis, mycardial infarction within 6 weeks, etc；
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Uncontrollable hypertension by medication (Systolic pressure≥ystolic pres diastolic blood pressure≥pressurec；
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Severe combined or unstable conditions, such as severe heart failure, lung failure or kidney failure (serum creatinine>3.0mg/dL (264 μmol/L) or renal cyspheric filtration rate (GFR) <30ml/min), severe liver insequencies, malignant tumors;
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A history of gastrointestinal haemorrhage or haemorrhagic disease (e.g. idiopathic platelet reduction cyanosis, etc.) or a history of bleeding tendencies within 6 months prior to the signing of the informed consent；
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Hemoglobin is below 90g/L, plateplates<90×109/L；
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The International Standardized Rate (INR) >1.5, with unreal corrective bleeding factors；
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Can not carry out antiplatelet/anticoagulant treatment, with anaesthetic and contrast agent contraindication;
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The angiography shows that the vascular path is curly, and the device is difficult to reach the target position or to withdraw；
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Patients known to be allergic to heparin, paclitaxel, contrast, aspirin and clopidogrel, anesthetics;
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Life expectancy is less than 1 year；
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Participants in other drug or device clinical trials that have not been completed；
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A pregnant or lactating woman, or a person planning to become pregnant within one year；
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Other conditions that the researchers consider patients are not suitable.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Henan Provincial People's Hospital | Zhengzhou | Henan | China |
Sponsors and Collaborators
- Yinyi(Liaoning) Biotech Co., Ltd.
- Henan Provincial People's Hospital
Investigators
- Principal Investigator: Tianxiao Li, Henan Provincial People's Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- LNYY2020001