Last updated: June 1, 2022
Sponsor: jiaoliqun
Overall Status: Active - Recruiting
Phase
N/A
Condition
Organ Transplant
Thrombosis
Cerebral Ischemia
Treatment
N/AClinical Study ID
NCT04695236
ASPIRE
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age between 18 and 80 years old
- Clinical signs consistent with acute ischemic stroke with large vessel occlusion inthe anterior circulation (internal carotid artery, middle cerebral artery M1 or M2segment)
- ASPECTS score 0-10
- Arterial puncture could be performed within 24 hours from symptom onset or LKN
- Baseline NIHSS (NIHSS) score prior to randomization ≥ 10 and NIHSS 1a ≥ 1
- Candidate for endovascular thrombectomy therapy in accordance with best practices perAHA standard stroke guidelines meeting all labeling requirements for EVT in the trial
- Successful recanalization of occluded vessel (mTICI 2b-3) after EVT
- No intracranial hemorrhage postoperative CT examinations immediately afterrecanalization. If the subject' recanalization of vessel could not achieve mTICI 2b-3,the subject could not enter the per-protocol analysis and will separate another group
- Informed consent form signed by subjects or their legal guardian
Exclusion
Exclusion Criteria:
- Subject who suffer serious infection (e.g. sepsis) or multiple organ failure
- Known presence of an IVC filter
- End stage renal disease on hemodialysis
- Known hypersensitivity to antiplatelet agents, anticoagulation drugs, iodinatedcontrast and/or anesthetics
- Known hypersensitivity to the components of the medical device
- Any known history of the following conditions: bleeding diathesis, coagulopathy,cryoglobulinemia, sickle cell anemia, will refuse blood transfusions orcontraindication to heparin; history of genetically confirmed hypercoagulable syndrome
- Use of warfarin with INR > 3
- Hemodynamically significant cardiac dysrhythmias (eg. QTc interval >450 msec,bradycardia (heart rate less than 50), Mobitz Type II second degree AV block (orhigher AV block), and severe ventricular dysrhythmias (sustained VT or VF)) whichcause significant hypotension (SBP ≤ 120 mmHg requiring more than two pressormedications)
- Platelet count<40×10^9/L
- Blood glucose concentration <2.7 or > 22.2 mmol/L
- Hypertension uncontrollable by drug treatment (systolic blood pressure≥185 mmHg ordiastolic blood pressure≥110mmhg)
- Expected life expectancy<6 months
- Temperature < 35°C on admission to Emergency Department
- With a pre-existing neurological or psychiatric disease that would confound theneurological or functional evaluations (e.g., dementia or mental illness)
- Subject participating in a study involving an investigational drug or device thatwould impact the current study
- Baseline CT/MR evidence of multiple vascular territory acute stroke
- Baseline CT/MR showing evidence of arterial vasculitis or dissection
- Evidence of intracranial hemorrhage or hemorrhagic transformation before thrombectomy
- Evidence of intracranial hemorrhage or hemorrhagic transformation immediately afterthrombectomy
- Presence of pulmonary embolism, ilio-femoral or deep vein thrombosis
- Brain vascular lesion (e.g. aneurysm or arteriovenous malformation)
- Brain tumor or CNS infection
- Concurrent participation in a study involving an investigational drug or device thatwould impact the current study
- Female patient of childbearing potential who is known to be pregnant or lactating
- For other reasons, the researchers believe that the patient is not suitable forcontinued treatment
- Patients without a legally authorized representative to sign the consent form will beexcluded
Study Design
Total Participants: 80
Study Start date:
December 31, 2020
Estimated Completion Date:
December 31, 2022
Study Description
Connect with a study center
Xuanwu Hospital
Beijing,
ChinaActive - Recruiting

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