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Granulocyte-Colony Stimulating Factor Treatment for Acute Ischemic Stroke: A Randomized Control Trial Study Assessing Clinical and Radiological Responses

Granulocyte-Colony Stimulating Factor Treatment for Acute Ischemic Stroke: A Randomized Control Trial Study Assessing Clinical and Radiological Responses

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201208081584N2
Enrollment
72
Registered
2012-09-16
Start date
2012-09-01
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

Acute Ischemic Stroke. A stroke is caused by the interruption of the blood supply to the brain, usually because a blood vessel is blocked by a clot. This cuts off the supply of oxygen and nutrients, causing damage to the brain tissue.

Interventions

Intervention 1: Case group receives G-CSF, 10 microgram per kilogram of body weight subcutaneously. However the first dose will be prescribed via intra venous line. Intervention 2: Control group will
Treatment - Drugs
Placebo
Case group receives G-CSF, 10 microgram per kilogram of body weight subcutaneously. However the first dose will be prescribed via intra venous line.
Control group will receive placebo (normal saline, 0.1 ml per kg of body weight). Participation in the study doesn’t produce any avoidance for receiving standard treatment of stroke.

Sponsors

Vice chancellor for research, Tehran University of Medical Sciences
Lead Sponsor
Pooyesh darou Company
Collaborator

Eligibility

Sex/Gender
All
Age
40 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion Critria: Age: 40-80; stroke was confirmed by DWI; less than 24 hours of beginning of stroke; NIHSS scale: 4-24; Stroke in MCA territory Exclusion critria: hypersensitivity to E coli proteins or G-CSF; History of cancer; History of severe renal, liver and hematological diseases; More than 2/3 of MCA territory; Pregnancy; The patient is candidate for rTPA; Acute ICH; Lacunar infarction

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical sign and symptoms. Timepoint: first week, 2nd week, 1st and 2nd and 3rd months. Method of measurement: NIHSS scale,Barthel Index Scale Score, modified rankin scale.

Secondary

MeasureTime frame
Lesion volume. Timepoint: one week. Method of measurement: Brain MRI(DWI and PWI).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Hossein Harirchian

Tehran University of Medical Sciences

harirchm@sina.tums.ac.ir+98 21 6119 2424

Outcome results

None listed

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