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The efficacy of Cerebrolysin in the treatment of acute ischemic stroke

The efficacy of Cerebrolysin in the treatment of acute ischemic stroke

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138803272042N1
Enrollment
100
Registered
2009-08-29
Start date
2009-08-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral infarction. Cerebral infarction

Interventions

Intervention 1: Intervention: Cerebrolysin (30 mg for first 5 days during the first week and 10 mg for first 5 days in the second, third and fourth weeks) adding to routine therapy. Intervention 2: Co
Treatment - Drugs
Intervention: Cerebrolysin (30 mg for first 5 days during the first week and 10 mg for first 5 days in the second, third and fourth weeks) adding to routine therapy
Control: placebo in the same dose of the intervention group

Sponsors

Research Deputy, Shahid Beheshti University of Medical Sciences
Lead Sponsor
Cobel Darou
Collaborator

Eligibility

Sex/Gender
All
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients aged 45 to 85 years, the occurrence of acute cerebral ischemic attack (embolic or thrombotic), hospitalization during 12 hours of first symptoms of stroke, systolic blood pressure less than 200 and diastolic less than 100 mmHg Exclusion Criteria: recovery of neurologic symptoms after 4 hours of attack, hemorrhagic stroke or the occurrence of stroke in vertebrobasilar system with blood pressure =200/100 mmHg, seizures, Papilledema or rising intracranial pressure (RICP), neck stiffness or symptoms of brain stimulation, the condition of consciousness stupor and coma (GCS = 6), acute myocardial infarction, National Institutes of Health Stroke Scale (NIHSS) less than 7 and more than 24, hepatic or renal failure - heart failure, dementia initial appearance, acute infectious disease, doubt the Involvement in subsequent brain area (posterior circulation), pregnant women, symptoms of progressive neurologic defects, patients who are in other trials, patients received piracetam or calcium channel blockers (CCB), Patients who received r-TPA treatment during first 4 hours of symptoms

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical evaluation of motor ability (speech and motor ability of patients). Timepoint: daily. Method of measurement: MRS (Modified Rankin Scale), NIHSS (National Institutes of Health Stroke Scale).

Secondary

MeasureTime frame
Improvement in the understanding of patients during the treatment. Timepoint: On days 3, 7, 15 and 30. Method of measurement: Asessment of CGIS (Clinical Global Impression Scale), PGS (Patient Global Satisfaction Score) and MMSE (Mini-Mental State Exam) by neurologist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr kurosh Gharagozli

Shahid Beheshti University of Medical Sciences

gharagoz@sbmu.ac.ir+98 21 5541 7243

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026