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Clinical Trials/NCT04695236
NCT04695236
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A Prospective, Multicenter, Randomized Clinical Trial to Evaluate the Safety and Efficacy of Intravascular Hypothermia Therapy of Patients With Acute Ischemic Stroke

jiaoliqun1 site in 1 country80 target enrollmentDecember 31, 2020

Overview

Phase
N/A
Intervention
Not specified
Conditions
Hypothermia
Sponsor
jiaoliqun
Enrollment
80
Locations
1
Primary Endpoint
Intracranial hemorrhage conversion rate
Last Updated
3 years ago

Overview

Brief Summary

Acute ischemic stroke (AIS) has been one of the major causes of global mortality and morbidity. The superiority of endovascular therapy (EVT) over standard medical therapy in treating AIS due to large vessel occlusion (LVO) in the anterior circulation has been widely accepted. However, a critical concern is that even with an extremely high rate of successful recanalization (the modified thrombolysis in cerebral infarction [mTICI] score 2b-3) around 90%, nearly half of the patients failed to benefit from EVT. So, adjunctive therapy of EVT for neuroprotection is required.

From the previous domestic and foreign literatures, hypothermia can prevent and treat secondary injury caused by ischemia-reperfusion injury and cerebral edema of acute cerebral ischemia, so as to achieve the role of neuroprotection. In this study, intravascular cooling was performed as soon as possible with careful temperature control in patients receiving thrombectomy. The temperature was controlled at 33° C for 48-72 hours. This parallel controlled study is to systematically evaluate the feasibility and safety of adjunctive therapy using early intravascular hypothermia in AIS patients receiving mechanical thrombectomy. The results will clarify a potential modality for neuroprotection and hopefully provide new evidence in improving patient prognosis.

Detailed Description

In this study, the target subjects were AIS patients with successful recanalization (mTICI 2b-3). Early intravascular hypothermia neuroprotection therapy was given to patients after thrombectomy to evaluate its safety and effectiveness. The neuroprotection effect of endovascular hypothermia therapy is explored regarding several aspects, such as hemorrhagic conversion rate, cerebral edema, and neurological function recovery, with specific evaluation criteria described in detail in the following experimental design.

Registry
clinicaltrials.gov
Start Date
December 31, 2020
End Date
December 31, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
jiaoliqun
Responsible Party
Sponsor Investigator
Principal Investigator

jiaoliqun

Prof.

Xuanwu Hospital, Beijing

Eligibility Criteria

Inclusion Criteria

  • Age between 18 and 80 years old
  • Clinical signs consistent with acute ischemic stroke with large vessel occlusion in the anterior circulation (internal carotid artery, middle cerebral artery M1 or M2 segment)
  • 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 per AHA 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 after recanalization. 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 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, iodinated contrast 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 or contraindication 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 (or higher AV block), and severe ventricular dysrhythmias (sustained VT or VF)) which cause significant hypotension (SBP ≤ 120 mmHg requiring more than two pressor medications)
  • Platelet count\<40×10\^9/L
  • Blood glucose concentration \<2.7 or \> 22.2 mmol/L

Outcomes

Primary Outcomes

Intracranial hemorrhage conversion rate

Time Frame: 7 days after thrombectomy operation or discharge

ICH

Secondary Outcomes

  • NIHSS(24 hours, 7 days or discharge)
  • Rate of symptomatic intracranial hemorrhage (sICH)(7 days after thrombectomy operation or discharge)
  • The rate of functional independency (mRS 0-2)(90 days)
  • The rate of mortality (mRS 6)(90 days)
  • Modified Rankin scale (mRS)(90 days)
  • Infarct volume(5-7 days after thrombectomy operation or discharge)
  • Rate of malignant cerebral edema(7 days after thrombectomy operation or discharge)

Study Sites (1)

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