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Efficacy of Cerebrolysin as an Adjuvant Therapy Following Mechanical Thrombectomy in Patients with Large Vessel Occlusion Stroke: A retrospective study

Efficacy of Cerebrolysin as an Adjuvant Therapy Following Mechanical Thrombectomy in Patients with Large Vessel Occlusion Stroke: A retrospective study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202306562134107
Enrollment
50
Registered
2023-06-27
Start date
2024-04-22
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Nervous System Diseases

Interventions

IV cerebrolysin
Standard therapy only which is IV thrombolysis plus mechanical thrombectomy

Sponsors

Ain Shams University hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients with acute cardioembolic stroke as defined by TOAST classification. - Evidence of large vessel occlusion - NIHSS =10, - Underwent successful mechanical thrombectomy ± IV thrombolysis, after fulfilling the standard eligibility criteria.

Exclusion criteria

Exclusion criteria: - Patients aged more than 80 years old - Patients with epilepsy - Patients who are pregnant or lactating - Patients serious, advanced, or terminal illness or life expectancy = 6 months - Patients with bleeding tendency or platelet count less than 100,000/uL - Patients with high INR above 1.7 - Patient receiving low molecular weight heparin therapy less than 24 hours of stroke onset. - Patient with premorbid cognitive impairment

Design outcomes

Primary

MeasureTime frame
The Primary outcome measure will be the overall proportion of subjects receiving Cerebrolysin compared to the control group experiencing a favorable functional outcome (by modified Rankin Scale0–2 and MOCA score) at 90 days, following stroke onset.

Secondary

MeasureTime frame
The Secondary outcomes are to determine the efficacy of Cerebrolysin as compared to the control group in reducing the risk of symptomatic secondary hemorrhagic transformation, improving neurological outcomes(NIHSS 0–2 at day 14, day 30, and 90), reducing mortality rates (over the 90-day).

Countries

Egypt

Contacts

Public ContactAyman El Sudany

Lecturer of neurology Ain Shams university

aymanhsudany@gmail.com+201110805581

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026