Clinical Trial Details
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NCT02768571 : Effects of Cerebrolysin Combined With Rehabilitation on Motor Recovery in Stroke
PhasePhase 4
AgesMin: 19 Years Max: 80 Years
Inclusion Criteria:

1. The first-ever stroke (ischemic)

2. Confirmed by CT or MRI

3. Subacute stage: less than 1 week

4. Severe motor function involvement (FMA < 50)

5. Age: between 19 and 80 years

6. Inpatients

7. Written informed consent obtained from the patient or legally authorized

Exclusion Criteria:

1. Contraindication of MRI

2. Progressive or unstable stroke

3. Pre-existing and active major neurological disease

4. Pre-existing and active (e.g., on chronic medication) major psychiatric disease, such
as major depression, schizophrenia, bipolar disease, or dementia

5. A history of significant alcohol or drug abuse in the prior 3 years

6. Advanced liver, kidney, cardiac, or pulmonary disease

7. A terminal medical diagnosis consistent with survival < 1 year

8. Substantial decrease in alertness at the time of randomization, defined as score of 2
on NIH Stroke Scale

9. Pregnancy or lactating; note that a negative pregnancy test will be required if the
patient is a female in reproductive years

10. Any condition that would represent a contraindication to Cerebrolysin, including
allergy to Cerebrolysin

11. Current enrolment in another therapeutic study of stroke or stroke recovery

12. Total serum bilirubin > 4 mg/dL, alkaline phosphatase > 250 U/L, SGOT/AST > 150 U/L,
SGPT/ALT > 150 U/L, or creatinine > 3.5 mg/dL; or cardiopulmonary deficits large
enough to interfere with reasonable participation in physiotherapy during the trial.

13. Previous porcine brain peptide administration history
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