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Study · Case report or series · n = 1 · 2021

2 results

Role of Cerebrolysin® in Rehabilitation in Ischemic Stroke: A Case Report.

Chanubol R, Lertbutsayanukul P

The American journal of case reports8 Sept 2021Cited by 6 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC-ND. Results still quote short attributed sentences.

Results from this study2

2 results from studies that gave the peptide. 2 results from people.

  1. 01HumanCase report or seriesEfficacy outcome

    In a patient with ischemic stroke, all assessment scores (NIHSS, mRS, MBI, ambulation) improved at 1, 3, and 6 months after Cerebrolysin given with rehabilitation.

    In plain wordsIn a patient with stroke, all assessment scores improved at 1, 3, and 6 months after Cerebrolysin given with rehabilitation.

    Outcome
    Direction not reportedStroke assessment scores (NIHSS, mRS, MBI, ambulation)
    Study

    n = 1

    Outcome group
    Neuroprotection · Nervous system and cognition
    Studied dose
    30 mL · intravenous · 10 daysAs given in this study (human).

    Source sentences

    Summary
    After Cerebrolysin® administration, the patient demonstrated improvement in all assessment scores at 1, 3, and 6 months.
    2 context sentences
    Summary · context
    After the post-stroke recovery plateau, the patient received 10 days of 30 mL intravenous Cerebrolysin® to support further neuro-recovery, together with long-term rehabilitation.
    Summary · context
    We utilized clinical standard assessment tools, including National Institutes of Health Stroke Scale (NIHSS), modified Rankin scale (mRS), modified Barthel Index (MBI), and function of ambulation, to evaluate the outcome of the patient, together with the adverse events monitoring.
  2. 02HumanCase report or seriesSafety outcome

    In a patient with ischemic stroke receiving Cerebrolysin, no serious adverse effects occurred.

    In plain wordsIn a patient with ischemic stroke receiving Cerebrolysin, no serious adverse effects occurred.

    Outcome
    Not applicableSerious adverse effects
    Study

    n = 1

    Outcome group
    Adverse events · Nervous system and cognition
    Studied dose
    30 mL · intravenous · 10 daysAs given in this study (human).

    Source sentences

    Summary
    No serious adverse effects were observed.
    2 context sentences
    Summary · context
    After the post-stroke recovery plateau, the patient received 10 days of 30 mL intravenous Cerebrolysin® to support further neuro-recovery, together with long-term rehabilitation.
    Summary · context
    We utilized clinical standard assessment tools, including National Institutes of Health Stroke Scale (NIHSS), modified Rankin scale (mRS), modified Barthel Index (MBI), and function of ambulation, to evaluate the outcome of the patient, together with the adverse events monitoring.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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