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STROKE RESEARCH TRIALS
Several clinical research studies are underway at the Chattanooga
Center for Neurolgic Research. The Center specializes in acute
and secondary stroke prevention trials. The following in a
summary of current research studies relating to stroke treatment
and prevention.
BAYx 3702
BAYx 3702 is classified as a neuroprotectant therapeutic drug.
During ischemic stroke, the immediate damage cannot be prevented
or treated. Complex biochemical cascades and axonal and neuronal
derangements follow ischemia, leading to delayed secondary
deterioration and poor outcome.
The massive release of glutamate following acute cerebral
ischemia results in a dramatic increase in the influx of calcium
into neuronal cells, resulting in cell death. Excitatory neurotransmitter
glutamate may also play a major role in secondary cell damage
following ischemic stroke.
The BAYx investigation attempts to determine whether this
medicine will act to prevent or reduce this highly deleterious
glutamate-induced activity.
A five-hour interventional window has been established for
this study, starting from the time stroke symptoms first manifest
to the initiation of therapy.
CHARISMA
Aspirin and the anti-platelet medication, Plavix, are combined
in this clinical trial to determine whether together, they
are more effective than either drug used individually.
DEDAS
The agent in this study is an advanced clot-buster
that dissolves vascular obstructions in the brain. Because
of its biochemical specificity, the drug used in DIAS is expected
to be safer and more effective than t-PA, causing less systemic
bleeding and hemorrhage.
FUJISAWA
Compound FK506 is currently approved as an immune suppressant
and anti-inflammatory agent that prevents tissue rejection
during organ transplants. During acute stroke these anti-inflammatory
properties may potentially reduce neuronal brain injury. up
to 12 hours after acute stroke onset. In this trial, FK506
may be administered either as monotherapy or else in combination
with t-PA.
RREACT/ONO
This is an acute stroke trial using a compound which inhibits
glial cell activation in the brain. Glial cells are thought
to play an inflammatory role in ischemic brain injury that
increases the size of the patients stroke. By inhibiting
glial cell activation this compound may decrease the ultimate
stroke area. Patients enrolled in this study must present
within onset of stroke symptoms less than six hours old. This
Phase II investigation will involve careful evaluation by
a neurologist and neuro-imaging with MRI scans of the brain.
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