Overview

Inhaled Nitric Oxide in Acute Ischemic Stroke Patients Undergoing Mechanical Thrombectomy

Status:
Not yet recruiting
Trial end date:
2024-06-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine the safety and feasibility of using inhaled nitric oxide (iNO) in patients undergoing intra-arterial mechanical thrombectomy (blood clot extraction or IAMT) for treatment of acute ischemic (non-bleeding) stroke (AIS).
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Wake Forest University Health Sciences
Collaborator:
Mallinckrodt
Treatments:
Nitrous Oxide
Criteria
Inclusion Criteria:

- Age 18 and < 80

- Clinical evidence of acute ischemic (non-bleeding) stroke (AIS) with NIH Stroke Scale
of 6 or higher

- Non-contrast Computed tomography (CT) Head with ASPECT (Alberta Stroke Program Early
CT) score 6

- Symptom onset began < 16 hours from initiation of intra-arterial mechanical
thrombectomy (IAMT) procedure

- CT Angiogram (CTA) evidence of anterior circulation MCA (Middle Cerebral Artery) M1
segment occlusion.

- CT Perfusion (CTP) evidence of core infarct volume of < 70ml and a ratio of ischemic
tissue to initial core infarct volume of 1.8 or greater, and an absolute volume of
penumbra of 15ml or greater

- Patient or patient's representative provides consent

- Pre-stroke modified Rankin Scale (mRS) of < =2

- General endotracheal anesthesia (GETA) is planned to be used, as standard care, for
IAMT

- Treatment with iNO requires mechanical ventilation. Because IAMT can be performed
using conscious sedation and not GETA, only those patients for which the procedure is
planned with GETA will be included. The decision for the type of anesthetic depends on
the severity of stroke, region of brain affected by the stroke, and the ability for
the patient to cooperate for the procedure.

Exclusion Criteria:

- Hypotension at presentation, defined as systolic blood pressure (SBP) < 100 or MAP <
60; profound hypertension with SBP >185 or DBP >110mmHg unable to be controlled with
IV medications

- Inability to undergo a brain MRI (e.g., implanted pacemaker)

- Patients who received IV tPA >4.5hrs after symptom onset

- Coaguloapathy, defined as platelet count < 50,000, INR >3.0, PTT > 3x normal, use of
novel anticoagulants with eGFR < 30ml/min

- Vulnerable Subjects including: mentally ill or incompetent patients, those with
diminished decision-making capacity, prisoners, inpatient care for long-term chronic
illness, terminally ill, pregnant women, and children

- Any form of hemorrhage on non-contrast CT Head or mass lesion

- Severe head injury within 90 days

- Pre-existing severe neurological/psychiatric disease

- Seizure at stroke onset (unable to assess NIHSS)

- Blood glucose < 50mg/dL or >400mg/dL

- Hemoglobin <7mmol/L

- eGFR < 30ml/min

- Allergy to contrast media

- Presumed septic embolus as source of stroke

- Flow limiting intracranial or extracranial carotid stenosis, or complete carotid
occlusion