Cerebral Infarction Clinical Trial
Official title:
"Evaluation by Transcranial Magnetic Stimulation of the Benefit of Fluoxetine on Motor Recovery After Stroke"
The objective of this study is to better characterize the mechanisms of action of fluoxetine
in motor recovery and more specifically to identify the neurophysiological substrate
underlying fluoxetine-induced motor recovery in stroke.
In this study, the investigators propose to use transcranial magnetic stimulation (TMS) to
assess the effect of a chronic treatment of fluoxetine on corticospinal excitability and
integrity.
Recently, a phase IIb clinical trial (Chollet et al., 2011 - FLAME study) revealed that early
administration of standard-dose oral fluoxetine (a selective serotonin re-uptake inhibitor
widely used as antidepressant) to patients with subacute ischaemic stroke and moderate to
severe motor deficit in the upper extremity enhanced motor recovery after 3 months, as
assessed by the Fugl-Meyer motor scale, suggesting that fluoxetine could be a promising drug
to promote recovery in stroke patients. However, the mechanisms, and their specificity, by
which fluoxetine improves motor function after stroke remain poorly understood.
The overall objective of this proposal is to better characterize the mechanisms of action of
fluoxetine in motor recovery and more specifically to identify the neurophysiological
substrate underlying fluoxetine-induced motor recovery in stroke.
The corticospinal system plays a key role in voluntary activation of upper limb muscles. Its
integrity has been related to spontaneous (but incomplete) recovery after stroke. So far, the
effect of fluoxetine on corticospinal excitability and integrity has been poorly explored
although this drug appears promising to promote motor recovery.
In this study, the investigators propose to use transcranial magnetic stimulation (TMS) to
assess the effect of a chronic treatment of fluoxetine on corticospinal excitability and
integrity. The investigators believe that this approach will be suitable to determine the
mechanisms of action of this drug on motor recovery after stroke.
The investigators will assess in a double-blind, monocentric (Saint-Anne Hospital Stroke
center), randomised, placebo-controlled study, the effect of a chronic treatment of
fluoxetine on corticospinal excitability and integrity using TMS in 40 patients suffering
from ischaemic stroke with hemiplegia or hemiparesis affecting motor hand functions.
By coupling TMS, visuomotor grip tracking task and several clinical scales, the
investigators' results will allow a more system-specific assessment than the Fugl-Meyer motor
scale of fluoxetine-induced motor hand recovery in stroke. We believe that this study will
support the beneficial effect of fluoxetine to promote motor recovery in stroke and will open
new vistas for treatment options using fluoxetine in patients with motor impairments. It is
expected that this study will provide preliminary data that will be subsequently used to
design new, more focused, clinical trials.
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