Inhibitory rTMS in Dystonic Wilson Patients
NCT01980433 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2021-06-15
Summary
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.
Conditions
- Wilson Disease
- Movement Disorders
- Repetitive Transcranial Magnetic Stimulation
Interventions
- DEVICE
-
Repetitive Transcranial Magnetic Stimulation (rTMS)
Inhibitory 1 Hz rTMS, delivered to left somatosensory cortex during rest. Intervention is delivered during 20 minutes in one single session.
- OTHER
-
pre and post-rTMS electroencephalogram
to verify the absence of infraclinical seizures
- OTHER
-
WCRS
Writer's cramp rating scale
- OTHER
-
handwriting scale DPRE
handwriting in development and being evaluated by the NRC Wilson
- OTHER
-
visual analog scale of discomfort writing and parameters collected on touchpad
Sponsors & Collaborators
-
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Nathalie KUBIS, MD, PhD · Physiology Department, Lariboisière Hospital
-
Jean-Marc TROCELLO, MD · Neurology, Lariboisière Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2014-01-31
- Primary Completion
- 2015-07-31
- Completion
- 2015-07-31
Countries
- France
Study Locations
More Related Trials
-
Surround Inhibition in Patients With Dystonia
NCT00029601 ·Status: COMPLETED
-
Neuromodulation Therapy for Task-Specific Dystonia
NCT06422104 ·Status: COMPLETED ·Phase: NA
-
Experimental Therapeutics in Essential Tremor Using Transcranial Direct Current Stimulation
NCT01579435 ·Status: COMPLETED ·Phase: NA
-
Transcranial Magnetic Stimulation for Focal Hand Dystonia
NCT01792336 ·Status: TERMINATED
-
Accelerating TMS for Cervical Dystonia
NCT06328114 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Propensity to Develop Plasticity in the Parieto-Motor Networks in Dystonia From the Perspective of Abnormal High-Order Motor Processing
NCT02504905 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Transcranial Magnetic Stimulation (TMS) Studies of Dystonia
NCT00017875 ·Status: COMPLETED
-
Somatosensory Processing in Focal Hand Dystonia
NCT00579033 ·Status: UNKNOWN ·Phase: NA
-
Effect of Increasing Motor Cortex Inhibition on Task Specific Dystonia
NCT01823237 ·Status: SUSPENDED ·Phase: NA
-
Dual-Site Transcranial Magnetic Stimulation of the Supplementary Motor Area and Cerebellum for the Treatment of Essential Tremor.
NCT07344194 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Magnetic Resonance (MR) Guided Functional Ultrasound-Neurosurgery for Movement Disorders
NCT01698450 ·Status: COMPLETED ·Phase: PHASE1
-
Video-supervised Motor and Awareness Training in Writer's Cramp
NCT04611009 ·Status: RECRUITING ·Phase: PHASE2
-
Effectiveness and Reliability of Hypnosis in Stereotaxy
NCT03074422 ·Status: UNKNOWN ·Phase: NA
-
Brain Inhibition of Muscle Movement in Normal Volunteers
NCT00047957 ·Status: COMPLETED
-
Quantifying Motor Network Dynamics to Predict and Enhance Outcomes in Pediatric Dystonia
NCT07325175 ·Status: RECRUITING ·Phase: NA
-
Abnormal Movements, Cerebellum and Sensorimotor : Oculomotor Study
NCT01495897 ·Status: COMPLETED ·Phase: NA
-
Neurophysiology of Task-Specificity of Focal Hand Dystonia
NCT00309010 ·Status: COMPLETED
-
Accelerated TMS for Focal Hand Dystonia
NCT06015672 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Multimodal Electrophysiological Study of Cortico-subcortical Biomarkers of Tics in Tourette Syndrome
NCT06909656 ·Status: RECRUITING ·Phase: NA
-
Study of Brain-spinal Cord Neural Connectivity in Spasticity
NCT06281223 ·Status: RECRUITING
-
Can Short Latency Afferent Inhibition Give us Clues to Better DYT 1 Dystonia Treatments?
NCT01435681 ·Status: COMPLETED
-
Facial Expression Recognition of Emotion and Categorization of Emotional Words in Gilles de la Tourette's Syndrome
NCT00664300 ·Status: COMPLETED
-
Brain Function in Focal Dystonia
NCT00102999 ·Status: COMPLETED
-
Three-dimensional Analysis of Obliquus Capitis Inferior Muscle Function in the Rotatory Form of Cervical Dystonia
NCT05327985 ·Status: TERMINATED
-
Multimodal Investigation of Cortico-Basal Ganglia-Thalamo-Cortical Network Dynamics in Dystonic Patients With Deep Brain Stimulation
NCT06716983 ·Status: RECRUITING