IVIG in Acute Ischemic Stroke: A Pilot Study
| Status: | Completed |
|---|---|
| Conditions: | Peripheral Vascular Disease, Neurology |
| Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
| Healthy: | No |
| Age Range: | Any |
| Updated: | 2/4/2013 |
| Start Date: | August 2012 |
| End Date: | November 2013 |
The purpose of the study is to evaluate the ability of IVIG to affect the rate of
progression of brain ischemia, as evidenced by neuroimaging.
The results of an ongoing epidemiological study indicate that patients with primary
immunodeficiency (PID) on IVIG replacement therapy have an overall prevalence of stroke that
is 5 times less than in the general population. Even more striking is the absence of stroke
in IVIG-treated PID patients over 65, while in the same general population age group the
stroke prevalence goes up to 8.1%. This suggests that the degree of stroke protection
correlates with the length of IVIG treatment, since older PID patients have been treated
with IVIG significantly longer than younger ones.
Two pre-clinical studies demonstrated the effectiveness of IVIG preparations in improving
the clinical outcome of stroke and at the same time provided evidence of the role of
complement fragments in the pathogenesis of ischemia-induced brain damage. Scavenging of
these active fragments by IVIG is the likely mechanism of beneficial effect. In one of these
studies CSL's own Privigen preparation was used. Considering that it exhibited in-vitro
scavenging abilities more pronounced than several other IVIG preparations, and that its
in-vivo scavenging capacity was also proven in a relevant animal model, a need to test this
preparation in stroke patients is warranted. In addition, activation of complement and the
level of activated fragments in humans seem to correlate with the severity of the disease,
making them an ideal therapeutic target.
Inclusion Criteria:
1. Onset of neurological symptoms between 4.5 and 8 hours
2. Male or Female age 45 -65 years old
3. Score of 10-15 points on the National Institutes of Health Stroke Scale (NIHSS) with
clinical signs suggestive of ischemic stroke
4. Acute brain ischemia with a distinct penumbra (at least 20%), measured by magnetic
resonance perfusion imaging (PI) and diffusion-weighted imaging (DWI), in the
territory of the middle cerebral artery, anterior cerebral artery, or posterior
cerebral artery with a hemispheric distribution
5. Ability and willingness to provide informed consent and comply with study
requirements and procedures
Exclusion Criteria:
1. Eligibility for acute thrombolytic (rtPA) treatment
2. Normal brain MRI
3. Transient ischemic attack or rapidly improving neurological symptoms
4. Previous disability
5. Hemorrhagic stroke on brain MRI (T2*/SWI)
6. Ongoing infection defined by clinical and laboratory signs: an evidence-based
guideline will be followed to detect infectious complications (in short, physical and
laboratory measures including WBC, ESR, hsCRP, PCT, fever, abnormal urine, chest
X-ray or positive cultures)
7. Diagnosis of malignancy
8. Known sensitivity to any ingredients in the study drug or radiological contrast
material
9. Participation in another clinical trial within the past 30 days
10. Stroke in the previous 3 months
11. Chronic liver, kidney or hematological disease
12. Contraindications to MRI -Brain aneurysm clip, implanted neural stimulator, implanted
cardiac pacemaker or defibrillator, cochlear implant, ocular foreign body e.g. metal
shavings, other implanted medical devices: (e.g. Swan Ganz catheter) insulin pump,
metal shrapnel or bullet.
13. Diabetes
14. Hypertension
15. Females who are pregnant or breastfeeding
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