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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01980433
Inhibitory rTMS in Dystonic Wilson Patients (WILSTIM)
Study of Writing Improvement in Patients With Wilson Disease and Dystonia After One Session of Inhibitory Repetitive Transcranial Magnetic Stimulation
Wilson disease is a genetic disorder resulting in copper accumulation in liver, brain and eye. The neurologic complications include dystonic syndrome, which is a prolonged and excessive muscle activation responsible for abnormal postures. Hand dystonia prevents daily life activities such as writing, which is particularly disabling, since writing is the only mean of communication in these patients with significant slurred speech. Treatment is limited and only partially effective.
Low frequency (<or=1Hz) repetitive transcranial magnetic stimulation (rTMS) has shown inhibiting properties when applied over the cortex. Since dystonia has been correlated to hyperactivation of the neurons of the somatosensory cortex (SSC), we hypothesize that one single 20-minute session of 1 Hz rTMS applied on left SSC will improve writing of the right dystonic hand, assessed immediately at the end of the session.
Descripción general del estudio
Estado
Condiciones
Descripción detallada
This study investigates the handwriting performance of an homogeneous cohort of patients with Wilson disease and right handed dystonia, after one single inhibitory repetitive transcranial magnetic stimulation (rTMS). Fifteen patients with focal right hand dystonia will receive randomly either active or sham rTMS (1 Hz) to the left somatosensory cortex (SSC) in one single 20 minutes session. Handwriting performance will be measured immediately after this unique session (Visual analogic scale of subjective discomfort in writing, DPRE and WCRS scales, pen pressure and pen velocity measured on touchpad), compared to scores obtained 24 hours before the session. Three days later, the patient will receive the other session (sham rTMS or active rTMS) and the same parameters will be evaluated.
This is a single-center, randomized, crossover, prospective, clinical and double-blind study (the rTMS session is performed by the neurophysiologist, but the patient and the neurologist who will perform the handwriting evaluation are blind to the session).
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Ile De France
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Paris, Ile De France, Francia, 75010
- Hospital Lariboisière
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Wilson disease with focal right hand dystonia
- No modification of medical treatment for 6 months
- No botulinum toxin administration within the past four months
- Right handed
- Focal right hand dystonia
- Cerebral Magnetic Resonance performed the last 6 months with no other lesion than met in Wilson disease
- Over 18
- Insurance policy holder
- Informed consent
Exclusion Criteria:
- Pregnant woman
- Guardianship procedure
- Seizure history
- Other cerebral lesions on cerebral MRI than met in Wilson Disease
- Unable to stay quiet for 30 minutes
- Handwriting impossible
- Contra-indications to repetitive Transcranial Magnetic Stimulation
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación cruzada
- Enmascaramiento: Triple
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Experimental: Active rTMS
Repetitive Transcranial Magnetic stimulation: 1 Hz rTMS, delivered to left somatosensory cortex during rest.
Intervention is delivered during 20 minutes in one single session.
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Inhibitory 1 Hz rTMS, delivered to left somatosensory cortex during rest.
Intervention is delivered during 20 minutes in one single session.
to verify the absence of infraclinical seizures
Writer's cramp rating scale
handwriting in development and being evaluated by the NRC Wilson
|
Comparador falso: Sham rTMS
Placebo Transcranial Magnetic stimulation delivered to left somatosensory cortex during rest.
Intervention is delivered during 20 minutes in one single session.
|
Inhibitory 1 Hz rTMS, delivered to left somatosensory cortex during rest.
Intervention is delivered during 20 minutes in one single session.
to verify the absence of infraclinical seizures
Writer's cramp rating scale
handwriting in development and being evaluated by the NRC Wilson
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
immediate and significant improvement in writing
Periodo de tiempo: up to 1 week
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Improvement of handwriting performance immediately after one single 20 minutes session of inhibitory (1 Hz) repetitive transcranial magnetic stimulation over the left somatosensory cortex. quantitative test score of writing WCRS Active or sham stimulation will be randomly assigned to the patient and the other session will be performed 3 days later. |
up to 1 week
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
significant improvement in writing
Periodo de tiempo: up to 1 week
|
improvement of other quantitative test scores of writing (VAS subjective discomfort writing, DPRE scales and parameters measured on touchpad) after a single session of 1 Hz rTMS inhibitory to the left CSS , compared to the scores achieved in the 24 hours before the session of rTMS. Active or sham stimulation will be randomly assigned to the patient and the other session will be performed 3 days later. |
up to 1 week
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improvement of dystonia on the scale WDRS
Periodo de tiempo: up to 1 week
|
Assessing the improvement of dystonia on the scale WDRS after a single session of 1 Hz rTMS inhibitory to the left CSS, compared to the scores achieved in the 24 hours before the session of rTMS. Active or sham stimulation will be randomly assigned to the patient and the other session will be performed 3 days later. |
up to 1 week
|
correlation between the scores and the other parameters of disease severity
Periodo de tiempo: up to 1 week
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Assess whether age, disease duration and the presence of cortical atrophy are inversely correlated with the evolution of scores.
|
up to 1 week
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Nathalie KUBIS, MD, PhD, Physiology Department, Lariboisière Hospital
- Investigador principal: Jean-Marc TROCELLO, MD, Neurology, Lariboisière Hospital
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades del Sistema Digestivo
- Enfermedades metabólicas
- Enfermedades Cerebrales
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Enfermedades del HIGADO
- Enfermedades Genéticas Congénitas
- Enfermedades de los ganglios basales
- Enfermedades neurodegenerativas
- Metabolismo, errores congénitos
- Trastornos Heredodegenerativos, Sistema Nervioso
- Enfermedades Cerebrales Metabólicas
- Enfermedades Cerebrales Metabólicas Congénitas
- Metabolismo de metales, errores congénitos
- Trastornos del movimiento
- Degeneración hepatolenticular
Otros números de identificación del estudio
- P121105
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