Wireless Implantable Mandarin Chinese Speech Neuroprosthesis Evaluation (WISE)
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Clinical team Stairmed
- Número de teléfono: +86 021-80510178
- Correo electrónico: yumiao@stairmed.com
Ubicaciones de estudio
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Shanghai Municipality
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Shanghai, Shanghai Municipality, Porcelana
- Reclutamiento
- Huashan Hospital, Fudan University
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Contacto:
- Ying Mao, Ph.D
- Número de teléfono: +86 021 5288 8045
- Correo electrónico: maoying@fudan.edu.cn
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age 18 to 80 years (inclusive), any gender.
- Clinically diagnosed with speech disorders, including locked-in syndrome, severe dysarthria, aphasia with preserved auditory comprehension, or late-stage ALS-related language dysfunction, secondary to stroke, traumatic brain injury, amyotrophic lateral sclerosis (ALS), or other motor neuron diseases.
- The subject, or the subject with the assistance of their legal representative, is willing to follow the investigator's instructions, adhere to all protocol-specified procedures, and complete all required follow-up.
- The subject and their legal representative fully understand the purpose and significance of the trial; the subject voluntarily agrees to participate and signs the informed consent form
Exclusion Criteria:
- Subjects with any previously implanted metallic objects or devices (e.g., pacemakers, defibrillators, neurostimulators, cochlear implants), except for dental metal implants or implants assessed to have no impact on the trial.
- Subjects who have been on long-term anticoagulant or antiplatelet therapy prior to screening, with antiplatelet drugs discontinued for less than 2 weeks before surgery; or subjects with hematological or autoimmune disorders (e.g., aplastic anemia, systemic lupus erythematosus); or subjects with clinically significant coagulation test abnormalities during the screening period.
- Subjects assessed by an anesthesiologist to be unable to tolerate anesthesia and surgery.
- Subjects assessed by the investigator to have nervous system diseases (e.g., cerebrovascular lesions, intracranial infections, neurodegenerative diseases, epilepsy) or a history of craniocerebral trauma, resulting in severe brain function impairment or marked EEG abnormalities.
- Subjects with physiological or pathological conditions that may lead to poor healing of scalp wounds.
- Subjects in the acute infection phase or suffering from other severe infections.
- Subjects with cognitive impairment or psychotic symptoms.
- Subjects with severe dysfunction of vital organs (heart, lung, liver, kidney, etc.), malignant tumors or autoimmune diseases, who are deemed ineligible for this clinical trial by investigators.
- Subjects judged by investigators to have an expected survival time of less than 1 year.
- Subjects with drug abuse or alcohol dependence.
- Pregnant or breastfeeding women, or subjects planning to become pregnant during the trial period.
- Subjects currently participating in clinical trials of drugs or other medical devices.
- Subjects unable to understand or read Chinese.
- Other circumstances under which investigators consider the subject unsuitable to participate in this clinical trial
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Viabilidad del dispositivo
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
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Experimental: Implantation of the WRS
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WRS is a minimally invasive, wireless brain-machine interface system.
Subjects with speech disorders undergo implantation of WRS, receive brain-control training, and are followed up.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence of Device-Related Adverse Events
Periodo de tiempo: From implantation to Month 12
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Adverse events determined by the investigator to be related to the investigational device, recorded throughout the study period.
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From implantation to Month 12
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Incidence of All Adverse Events
Periodo de tiempo: From implantation to Month 12
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From implantation to Month 12
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Incidence of Device Deficiencies
Periodo de tiempo: From implantation to Month 12
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From implantation to Month 12
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Number of Reliable Recording Channels at Each Evaluation Time Point
Periodo de tiempo: At 3, 6, 9, and 12 months post-implantation
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At 3, 6, 9, and 12 months post-implantation
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Speech Output Rate in Characters Per Minute (CPM)
Periodo de tiempo: At 3, 6, 9, and 12 months post-implantation
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The speech output rate, defined as the number of Chinese characters produced per unit time during task performance, is calculated and documented every 3 months during the follow-up period.
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At 3, 6, 9, and 12 months post-implantation
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Speech Output Character Error Rate (CER)
Periodo de tiempo: At 3, 6, 9, and 12 months post-implantation
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The subject independently outputs the complete sequence of Chinese characters from a standard reference text.
The minimum edit distance (total substitutions, deletions, and insertions) between the decoded sequence and the reference sequence is divided by the total number of Chinese characters in the reference text to obtain the character error rate.
Recorded every 3 months during follow-up.
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At 3, 6, 9, and 12 months post-implantation
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- STAIRSUP-201
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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