Stroke Clinical Trial
Official title:
Safety and Long-term Effectiveness of High Frequency Repetitive Transcranial Magnetic Stimulation at the Subacute Phase of Ischaemic Stroke
The aim of the study is to determine if 2-week repetitive transcranial magnetic stimulation at the subacute phase of stroke (between day 7 and day 14) improves significantly arm motility at 3 months with remaining effect at one year, without significant adverse effect.
Stroke survivors may be left with disability involving speech or residual arm or leg
weakness. Despite spontaneous improvement on the weeks following stroke, the importance of
final disability is unpredictable. If the core of the infarct is represented by dead
neurons, the neurons from adjacent areas seem to be staggered and their lack of excitability
has been correlated to a bad prognosis. Repetitive transcranial magnetic stimulation (rTMS)
seems to be a promising technique since high frequency rTMS can increase excitability of the
targeted neurons.
The aim of the study is to evaluate after 2 weeks of 20 min of rTMS each day: 1) the
improvement of arm function and neurological and disability scales, immediately after the
2-week session, at one month, 3 months and evaluate the remnant effect at 12 months, 2) to
correlate these scales to physiological parameters in order to assess the clinical
modifications to the electrophysiological modifications, 3) to assert the safety of high
frequency rTMS at the subacute phase of ischaemic stroke.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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