REperfusion With Cooling in CerebraL Acute IscheMia II

This study is designed to examine the safety and proof of concept of therapeutic hypothermia
prior to conventional revascularization in subjects experiencing acute ischemic stroke by
comparing the results to subjects who remain at normal body temperature (normothermic) and
proceed directly to reperfusion via conventional reperfusion intervention.

The investigational plan also examines the following outcomes in 85 subjects randomized to
either hypothermia or normothermia:

- Regulation of biomarkers indicative of ischemia-reperfusion injury

- Changes in blood brain injury using the Hyperintense Acute Reperfusion Marker (HARM)
protocol MRI as a surrogate imaging biomarker

- Incidence of hemorrhagic conversion post reperfusion

- Neurologic function at 90 days post acute ischemic stroke.

The results of this study will be used to power a definitive phase III clinical trial
evaluating the combination of hypothermia and revascularization versus reperfusion alone.

Inclusion Criteria:

- Male or female subjects of any ethnicity and age >/=18 but
- Symptom onset
- Symptoms consistent with an ischemic stroke with a large vessel occlusion (Middle
Cerebral Artery (MCA), Internal Carotid Artery (ICA) terminus) as determined by CT
imaging of the brain;

- Alberta Stroke Program Early CT Score (ASPECTS) of 5-10 on non-contrast CT of the
brain;

- Ability to undergo endovascular reperfusion therapy;

- No contraindications to general anesthesia, conscious sedation, or allergies to any
components associated with the anticipated diagnostic or treatment procedures that
cannot be treated;

- A pre-treatment modified Rankin Scale (mRS) of 0 or 1;

- Baseline CT scan shows no hemorrhage;

- National Institutes of Health Stroke Scale (NIHSS) 14-29;

- Subject has either 1) failed iv tissue plasminogen activator (tPA) therapy or 2)
contradicted for iv tPA therapy;

- Subject is capable of complying with study procedures and agrees to complete all
required study procedures, study visits and associated activities.

- Subject or legally authorized representative must be able to understand and give
written informed consent.

Exclusion Criteria:

- Females of childbearing potential who are pregnant or not using adequate
contraception;

- Bleeding diathesis with a platelet count < 50,000 or International Normalized Ratio
(INR) >1.7 or any active or recent (within 10 to 30 days) hemorrhage;

- History of genetically confirmed hypercoagulable syndrome;

- Any condition that excludes MRI imaging;

- History of dementia, currently on Aricept or Namenda, or other Alzheimer's-like
symptoms;

- End stage renal disease on hemodialysis;

- History of cardiac arrest;

- Presence of an inferior vena cava (IVC) filter;

- Contrast dye allergy with history of anaphylaxis, known serious sensitivity to
contrast agents or any condition in which angiography is contraindicated;

- Known allergy to meperidine or buspar;

- Prior neurologic event that would obscure interpretation of the signal and current
presenting neurologic deficits;

- Sustained hypertension (systolic blood pressure (SBP) > 185 or diastolic blood
pressure (DBP) > 110 refractory to treatment);

- Baseline CT/MRI of head showing evidence of mass effect with mid-line shift,
hemorrhage, intracranial tumor, arterial vasculitis or dissection, or bilateral
stroke;

- Presence of any other serious comorbidity that would be likely to impact life
expectancy to less than 6 months or limit subject cooperation or study compliance;

- Concurrent participation in an investigational clinical study that has not completed
the follow-up period or planned participation in another study within the next 3
months;

- Any other condition or personal circumstance that, in the judgment of the
investigator, might interfere with the collection of complete, good quality data or
the completion of the research study.