In severe subacute stroke patients, no adverse events occurred in the Cerebrolysin or placebo groups.
In plain wordsIn severe subacute stroke patients, no adverse events occurred in either the Cerebrolysin or placebo group.
- Peptide
- Cerebrolysin
- Outcome
- No significant changeAdverse events
- Study
n = 60
- Outcome group
- Adverse events · Whole body
- Studied dose
- Dose not stated
Source sentences
There were no adverse events.
2 context sentences(design, population, supporting numbers)
A randomized, double-blind, placebo-controlled study was conducted.
Sixty patients at the early stage of severe sub-acute stroke who fulfilled all eligibility criteria were randomly assigned to the Cerebrolysin group or placebo group (𝑛 = 30 each).