The first phase consists of a temporary trial period intended to verify the clinical effectiveness of the system and the improvement in pain before the final implant.
The procedure is performed under intravenous sedation and local anesthesia. Using high-precision radiological guidance, one or more electrodes are implanted in the cervical, thoracic, or lumbar epidural space, depending on the location of the pain.
The electrodes are temporarily connected to an external stimulator that the patient will use for several days or weeks, allowing the clinical response to be evaluated and the stimulation programming to be optimized.