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Therapeutic Areas: Neurology | Hematology | Cardiology/Vascular Diseases | Family Medicine
 Disease Category: Stroke
Location: United States, WA

Trial Information

Are you experiencing deficits post ischemic stroke?

We are investigating a medication that may improve sensorimotor function in patients who have stabilized with long term residual deficits following stroke.

Patient Inclusion Criteria

  • History of a stable sensorimotor deficit due to an ischemic stroke, as confirmed by the Investigator with supportive prior imaging findings (MRI/ CT scan), ≥ 6 months post-stroke
  • Men or women aged 18 to 85 years inclusive
  • Have sufficient ambulatory ability to complete T25FW at Screening Visit and every other visit as required

Patient Exclusion Criteria

  • History of seizures, except simple febrile seizures
  • Orthopedic surgical procedures in any of the extremities within the past 6 months
  • There are other study requirements that will determine whether individuals may participate in this clinical research study.

Kathy Hendricks, AS, CCRC, Site Manager
Clinical Trials of America, Inc
914 Lawton Road
Lynnwood, WA 98036
Phone: 206-769-3175
Email: kathyh@ctofa.com

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Research Center Information: Clinical Trials of America, Inc

If you would like to learn more about participating in this study, please send an email message using the form below.

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