About this trial
The objective of this study is to evaluate the safety and efficacy of minimally invasive, wireless brain-machine interface system (WRS) in patients with paralysis (resulting from spinal cord injuries, brainstem strokes, amyotrophic lateral sclerosis, or other motor neuron diseases causing complete or incomplete quadriplegia) or bilateral upper limb amputations. By leveraging brain-machine interface alternative technology, participants can use brain signals to control external devices (such as moving cursors, wheelchairs, robotic arms, WeChat Mini Programs, and other physical assistive devices), thereby improving their motor function and quality of life.
Eligibility criteria
Qualifiers
Adults aged 18-65 years;
Patients with complete or incomplete quadriplegia due to spinal cord injury, brainstem stroke, amyotrophic lateral sclerosis (ALS), or other motor neuron diseases, or those with bilateral upper limb amputations;
Normal motor cortex function confirmed by neurological assessment;
Muscle strength of bilateral or unilateral upper limbs ≤ Grade 3;
Disqualifiers
Patients with neuropsychiatric disorders or psychological impairments;
Patients with brain MRI findings showing hemorrhage, tumors, anatomical abnormalities, or distortions;
History of severe systemic diseases (e.g., cardiac, pulmonary, hepatic, renal, thyroid, gastrointestinal, or hematologic disorders), poorly controlled diabetes, or pregnancy in females;
History of infectious diseases (e.g., syphilis, HIV), severe traumatic brain injury, or major surgeries;
Trial design
Treatments tested in this trial
- Implant