Acute stroke. Cerebral infarction, unspecified
Conditions
Interventions
Intervention 1: Control group: Participants will receive capsules containing microcrystalline cellulose as a placebo orally once a day for 90 days along with physical therapy one hour a day, 5 days a
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Over 18 years old motor or sensory paralysis of half of the body following the first episode of acute stroke (within the last 24 hours), cerebral ischemia Vogel-Meyer motor score below 55
Exclusion criteria
Exclusion criteria: Age over 70 years National Institute of Health stroke score above 15 Previous disabilities include: lack of speech, cognitive and movement disorders caused by stroke or any disease of the cerebral cortex. Pregnancy or breastfeeding Current use of antidepressants Kidney failure (glomerular filtration rate below 30 ml per minute) Abnormal liver function tests Hyponatremia and long TQ interval in heart strip Restlessness, increased pressure or other manifestations of serotonin syndrome (after starting treatment)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Motor function after acute stroke in patients. Timepoint: On the 90th day from the beginning of the study. Method of measurement: Fugl-Meyer movement scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Vahid Dehghani
Kashan University of Medical Sciences
Outcome results
None listed