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By invitation only Not applicable NCT07018388

Intrapatient Comparison of STN and GPi tTIS in PD

No applicable phase (e.g. observational)
Conditions: Parkinson Disease

Sponsor: Ruijin Hospital

trial.available_in: БГ
Overview
The goal of this clinical trial is to investigate the therapeutic efficacy of tTIS in patients with Parkinson's disease and to evaluate the immediate effects and conduct intrapatient comparisons of individualized 130 Hz Subthalamic Nucleus-transcranial Temporal Interference Stimulation (STN-tTIS) and Globus Pallidus Internus-transcranial Temporal Interference Stimulation (GPi-tTIS) on motor symptoms in patients with early to mid-stage Parkinson's Disease (PD) during "off" medication states. The main questions this study aims to answer are: 1. Can tTIS significantly improve the motor symptoms of patients with Parkinson's disease? 2. Is the therapeutic effect of STN-tTIS superior to that of GPi-tTIS?
Description
This clinical trial aims to verify the efficacy of tTIS in patients with Parkinson's disease and to explore which targets are better for improving PD motor symptoms.Patients were randomly assigned to receive Stimulation Type A, B, or C. Type A received STN-tTIS therapy; Type B received GPi-tTIS therapy; Type C received sham stimulation targeting the subthalamic nucleus. Each session lasted 20 minutes, and patients were in the off-medication state for all treatments.The order of stimulation types was randomized, with at least 7 days of washout between sessions to avoid carryover effects. MDS-UPDRS-III evaluations were assessed before and after each treatment.
Who can participate
Inclusion Criteria: * Diagnosis of primary Parkinson's disease (MDS); * Hoehn \& Yahr stage ≤ 3; * Antiparkinsonian drugs must have remained unchanged in the past four weeks, and the dosage must have remained stable throughout the study. Exclusion Criteria: * Presence of neurological disorders that may affect the study (e.g., traumatic brain injury); * Antipsychotics, antidepressants, or dopamine modulators outside of PD drugs; * Metal devices in the head or heart (e.g., deep brain stimulators, pacemakers); * Unstable vital signs.
Interventions
NervioX-2400
DEVICE
NervioX-2400
DEVICE
NervioX-2400
DEVICE
Locations 1
China (1)
Ruijin Hospital
Shanghai , Shanghai Municipality
Technical details
Status
By invitation only
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
50 Years
Maximum age
85 Years
Healthy volunteers
No
Start date
23.04.2025
Completion date
01.11.2026
Registry ID
NCT07018388
Source
clinicaltrials.gov
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