Interleaving Stimulation Improves Dyskinesia in Parkinson's Disease

Status Recruiting

Clinical Trial Summary

Clinical Trial Description

This study is designed as a prospective, randomized, double-blind, controlled study to assess putative differences in the effect of interleaving stimulation and empirical stimulation with regards to post-operation dyskinesia control. The primary objective is to assess putative differences in the effect of interleaving stimulation and empirical stimulation with regards to dyskinesia control. 50 Patients will be randomly assigned to either the interleaving stimulation modes group (ISG) or the empirical stimulation modes group (ESG). In ISG, empirical stimulation for the first 3 months, followed by interleaving programming period for 6 months, and any stimulation decided by the neurologists/neurosurgeons for the final 3 months. In ESG, empirical programming for the first 9 months' period, followed by any stimulation decided by the neurologists/neurosurgeons for the final 3 months. The change of dyskinesia scores (UPDRS IV, item 32 + item 33), Parkinson's disease quality of life-39 (PDQ-39) scores, scores of United Parkinson's Disease Rating Scale Part III as well as scores of neuropsychological Battery in interleaving stimulation compared to empirical programming modes will be measured based on corresponding time frame. Finally, the results will be analyzed via proper statistical methods and thus the conclusion will be drawn. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06239454
Study type	Interventional
Source	Huashan Hospital
Contact	Jian-Jun Wu, MD
Phone	86-21-52888163
Email	jungliw@gmail.com
Status	Recruiting
Phase	N/A
Start date	March 1, 2022
Completion date	February 28, 2025

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