About this trial
To evaluate the safety and efficacy of a Minimally Invasive Wireless Implantable Brain-Computer Interface (BCI) System NEO in patients with tetraplegia and to provide a basis for product registration.
Through brain-computer interface alternative technology, patients can control the external equipment with brain signals to improve the patient's quality of life.
Eligibility criteria
Qualifiers
Age between 18 and 65 years old, no restriction on gender.
Tetraplegia caused by cervical spinal cord injury.
Score of ≤1 on either the ball grasp or water pouring tasks of the ARAT (Action Research Arm Test).
Muscle strength of finger flexors < grade 3 according to ISNCSCI (International Standards for Neurological Classification of Spinal Cord Injury).
Disqualifiers
Without the consent of the patient or the patient's legal guardian.
Presence of syringomyelia, severe neuropathic pain, or severe spasticity that limits the participant's ability to engage in training.
Requires ventilator support.
Baclofen dosage >30 mg/day.
Trial design
Treatments tested in this trial
- NEO
Treatment groups
Sponsors and collaborators
Neuracle Medical Technology(Shanghai) Co.,Ltd.
Lead sponsor
Huashan Hospital
Collaborator
Xuanwu Hospital, Beijing
Collaborator
The First Affiliated Hospital with Nanjing Medical University
Collaborator
First Affiliated Hospital of Fujian Medical University
Collaborator
Beijing Tiantan Hospital
Collaborator
Henan Provincial People's Hospital
Collaborator
West China Hospital
Collaborator
Affiliated Hospital of Nantong University
Collaborator
The General Hospital of Eastern Theater Command
Collaborator
Peking University Third Hospital
Collaborator
Xiangya Hospital of Central South University
Collaborator
Tongji Hospital
Collaborator