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Clinical Trial Summary

Primary cranial-cervical dystonia is managed mainly by repeated botulinum toxin injections.This study is to establish whether subthalamic nucleus neurostimulation could improve symptoms in patients not adequately responding to chemodenervation or oral drug treatment. Investigators compared this surgical treatment with sham stimulation in a randomized, controlled clinical trial.


Clinical Trial Description

In this randomised, sham-controlled trial, investigators will recruit forty patients with primary cranial-cervical dystonia to receive an implanted device for STN-DBS, and participants will be randomly assigned to receive either neurostimulation or sham stimulation for 3 months.The primary end point was the change from baseline to 3 months in the severity of symptoms, according to the Burke-Fahn-Marsden Dystonia Rating Scale. Two masked dystonia experts who unaware of treatment status will assess the severity of dystonia by reviewing standardised videos.Subsequently, all patients will receive open-label neurostimulation; blinded assessment will be repeated after 6 months of active treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02583074
Study type Interventional
Source Beijing Tiantan Hospital
Contact Zhang Kai, MD
Phone 861067096767
Email zhangkai62035@163.com
Status Recruiting
Phase N/A
Start date September 15, 2015
Completion date December 31, 2018

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