The purpose of this non-interventional, exploratory trial is to document in 20 stroke patients the simplicity of handling and safety of transcranial laser needle stimulation with the Weberneedle®-System in the treatment of subacute ischemic stroke in daily routine practice. Treatment with laser needle stimulation is initiated within one week after onset of stroke; it will be applied once daily for 20 minutes for 5-10 days depending on the length of hospital stay of the patient. Safety and the neurological outcome (National Institutes of Health Stroke Scale (NIHSS), Rankin Scale, Bartel Index, Mini–Mental State Examination (MMSE)) will be observed over a period of 90 days.
|Duration||01/07/2012 - 31/12/2020|
|Funding||Private (Stiftungen, Vereine etc.)|
|Principle investigator for the project (University for Continuing Education Krems)||Assoziierte(r) Prof. Dr. Yvonne Teuschl|
|Project members||Dr. Martina Reiter, MSc|