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CNI Stroke Program

Research & Outcomes

Clinical Trials

StELLAR: enrolling

To assess the safety and preliminary efficacy of combining intravenous tPA with transcranial laser therapy (TLT) with the NeuroThera® Laser System in subjects treated for acute ischemic stroke.

Inclusion Criteria:

Subjects will be eligible if the following criteria are met:

  • Between 40 and 80 years of age
  • Subject has received IV rt-PA per the NINDS rt-PA Protocol Guidelines within 3 hours of symptom onset for an acute ischemic stroke and has a documented NIHSS score of > 7 and < 17 prior to IV rt-PA administration

Exclusion Criteria:

Subjects who meet any of the following criteria will be excluded from this study:

  • The subject had a seizure at stroke onset or within the 7 days prior to stroke onset.
  • The subject has an implant of any kind in the head (i.e. clipped aneurysm, embolised AVM, implantable shunt – Hakim valve).

Please contact Paula Fisk by e-mail or by phone at 303.806-7455.

___________________________________________

POINT: enrolling

This is a study to determine whether clopidogrel (Plavix) taken after a loading dose of 600 mg is effective in preventing major ischemic vascular events (stroke, myocardial infarction or ischemic vascular death) at 90 days when initiated within 12 hours of a TIA or minor ischemic stroke onset. Patients will also be receiving aspirin daily.

  • 18 years old
  • NIHSS of 3 or less
  • Must be treated within 12 hours from onset of TIA/stoke symptoms

Please contact Paula Fisk by e-mail or phone 303.806.7455.

___________________________________________

IMS III: enrolling

This trial examines whether combined intravenous (IV) and intra-arterial (IA) treatment is superior to standard IV rt-PA alone when started within three hours of stroke onset.

  • 18 – 82 years of age
  • NIHSS of 8 of higher
  • Must be able to initiate study medication within 3 hours from onset of stroke onset

Please contact Paula Fisk by e-mail or phone at 303.806.7455.

___________________________________________

DIAS-4: enrolling

A randomised, double-blind, parallel-group placebo-controlled phase III study to evaluate the efficacy and safety of desmoteplase in subjects with acute ischemic stroke.

  • Clinical diagnosis of acute ischemic stroke
  • Male or female between 18 and 85 years of age inclusive
  • Treatment of the subject can be initiated within 3 – 9 hours after the onset of stroke symptoms
  • NIHSS score 4-24

Please contact Paula Fisk by e-mail or phone 303.806.7455.

     
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