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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03381456
Other study ID # 2013_51
Secondary ID 2014-A00244-43
Status Completed
Phase N/A
First received December 18, 2017
Last updated December 18, 2017
Start date April 2015
Est. completion date April 2017

Study information

Verified date December 2017
Source University Hospital, Lille
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Cortical excitability depends on inhibitory mechanisms efficiency among which long latency intracortical inhibition (LICI) can be studied by paired pulses transcranial magnetic stimulation (TMS). Some recent evidences suggest that LICI may be one of the mechanisms by which the motor comment is adapted to the ongoing motor task with LICI strength being dependent on task complexity. In writer cramp and musician cramp, two forms of dystonia, the cortical excitability is not correctly modulated in some complex gestures. the hypothesis is that this task dependent perturbation of excitability in writer cramp could be due to a lack of LICI efficiency.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 2017
Est. primary completion date April 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Patient with hand dystonia : writers cramp

- Subject affiliated to social security regimen.

For healthy volunteers :

- Healthy volunteer without neurological disorders based on sensorimotor examination.

- Subject affiliated to social security regimen.

Exclusion Criteria :

- Subject unable to receive informed consent (dementia).

- Contraindication to Transcranial Magnetic Stimulation(TMS) (epilepsia, intracranial metalic foreign object, hearing device, cochlear implant).

- Patient using a psychotrope treatment.

- Patient under guardianship or curatorship.

- Pregnant or nursing women.

- Patient with a cardiac stimulator.

For healthy volunteers only :

• Abnormal neurological evaluation based on sensorimotor examination or neurological history ( epilepsy, stroke ; brain or spinal cord surgery ; history of neurological disease affective sensitive and motor control)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
LICI
Paired pulse TMS to measure LICI and late cortical disinhibition

Locations

Country Name City State
France Hôpital Roger Salengro, CHRU de Lille Lille

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Lille

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary long-interval intracortical inhibition (LICI) level Amount of inhibition at interstimulus intervals of between 50 to 300ms Baseline
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