Skip to main content
Clinical Trials/JPRN-UMIN000006607
JPRN-UMIN000006607
Completed
Phase 2

G-CSF employing neuroprotection study for ischemic stroke -Phase 2 clinical trial-(GENESIS-2) - G-CSF employing neuroprotection study for ischemic stroke -Phase 2 clinical trial-(GENESIS-2)

Tokai University, School of Medicine, Division of Neurology, Department of Internal Medicine.0 sites100 target enrollmentDecember 1, 2011

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
acute cerebral infarction
Sponsor
Tokai University, School of Medicine, Division of Neurology, Department of Internal Medicine.
Enrollment
100
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
December 1, 2011
End Date
October 12, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Tokai University, School of Medicine, Division of Neurology, Department of Internal Medicine.

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\.Splenomegaly or splenic lesions on echo. 2\.Leukocytosis more than 15000/mm3 3\.Past history of G\-CSF treatment. 4\.Plan for percutaneous angiography or bypass operations. 5\.Difficult to perform MRI. 6\.Past histries of symptomatic intracranial hemorrhage, bleeding tendency or coagulating disorders. 7\.Hyper reactivity to G\-CSF. 8\.Congestive heart failure or uncontrollable angina. 9\.Thrombocytopenia(less than 140000/mm3\) 10\.Liver dysfunction(AST(GOT),ALT(GPT) more than 100 IU/L) 11\.Renal dysfunction (creatinine 1\.5mg/dl and more) 12\.Difficult to continue this trial due to social problems, etc. 13\.Join other clinical trials. 14\.Inappropriate to enroll in this trial by the judgment of the doctor.

Outcomes

Primary Outcomes

Not specified

Similar Trials