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Inhibitory rTMS in Dystonic Wilson Patients (WILSTIM)

A

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Wilson Disease
Movement Disorders
Repetitive Transcranial Magnetic Stimulation

Treatments

Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
Other: visual analog scale of discomfort writing and parameters collected on touchpad
Other: handwriting scale DPRE
Other: WCRS
Other: pre and post-rTMS electroencephalogram

Study type

Interventional

Funder types

Other

Identifiers

NCT01980433
P121105

Details and patient eligibility

About

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.

Full description

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).

Enrollment

14 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

14 participants in 2 patient groups

Active rTMS
Experimental group
Description:
Repetitive Transcranial Magnetic stimulation: 1 Hz rTMS, delivered to left somatosensory cortex during rest. Intervention is delivered during 20 minutes in one single session.
Treatment:
Other: pre and post-rTMS electroencephalogram
Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
Other: visual analog scale of discomfort writing and parameters collected on touchpad
Other: WCRS
Other: handwriting scale DPRE
Sham rTMS
Sham Comparator group
Description:
Placebo Transcranial Magnetic stimulation delivered to left somatosensory cortex during rest. Intervention is delivered during 20 minutes in one single session.
Treatment:
Other: pre and post-rTMS electroencephalogram
Device: Repetitive Transcranial Magnetic Stimulation (rTMS)
Other: visual analog scale of discomfort writing and parameters collected on touchpad
Other: WCRS
Other: handwriting scale DPRE

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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