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Clinical Trial Summary

Repetitive transcranial stimulation (rTMS) of the posterior parietal cortex will be applied daily over five days in adult Gilles de la Tourette patients. This approach aims at reducing premonitory sensations believed to induce tics. Patients will be randomized to an active or placebo (sham) group in a crossover design.


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01043549
Study type Interventional
Source Institut National de la Santé Et de la Recherche Médicale, France
Contact
Status Terminated
Phase Phase 2
Start date February 2010
Completion date September 2012

See also
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Completed NCT05047705 - Investigating Distress Tolerance in Adults With Tourette Syndrome N/A
Recruiting NCT03914664 - Neural Correlates of Sensory Phenomena in Tourette Syndrome
Recruiting NCT06385535 - Clinical Characteristics and Temporal Properties of Individual Tics in Persistent Tic Disorder N/A