This research is a Randomized, double-blind, placebo-controlled, multicenter clinical study. Chinese subjects with Ischemic Stroke.
Subjects will randomly enter into one of two groups,the period of treatment is 14 days,follow-up to the 90th days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
216
Beijing Tiantan Hospital affilliated to Capital Medical University
Beijing, Beijing Municipality, China
To determination the proportion of subjects that 0-1 score of mRS after treatment 90 days
Time frame: 90 days
To compare treatment arms in terms of change from baseline to endpoint in NIHSS score.
Time frame: 90 days
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