This is a randomized, double-blind, placebo-controlled parallel group outpatient study that will utilize standard stroke rehabilitation outcome measures, as well as fMRI techniques in a subset of subjects, to evaluate the effect of HT-3951 on motor recovery and behavior in medically stable subjects following ischemic stroke.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
61
Unnamed facility
Phoenix, Arizona, United States
Unnamed facility
Scottsdale, Arizona, United States
Unnamed facility
Downey, California, United States
Fugl-Meyer Assessment of Upper Extremity, Part A-D
Time frame: 21-days
Index Finger-Tapping Frequency Test
Time frame: 21-days
Nine-Hole Peg Test
Time frame: 21-days
Hand Grip Strength Dynamometer Test
Time frame: 21-days
Arm Motor Ability Test-9
Time frame: 21-days
Stroke Impact Scale (hand domain)
Time frame: 21-days
Somatosensory evoked potential (if available)
Time frame: 21-days
Two-Minute Walk Test
Time frame: 21-days
Behavioral, neural activity and motor network connectivity levels, using functional MRI
Time frame: 21-days
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Unnamed facility
Glendale, California, United States
Unnamed facility
Loma Linda, California, United States
Unnamed facility
Orlando, Florida, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Grand Rapids, Michigan, United States
Unnamed facility
Kansas City, Missouri, United States
Unnamed facility
West Orange, New Jersey, United States
...and 8 more locations