MedPath

Frequency Associated Suppression of Tremor in Parkinson’s Disease and Essential Tremor

Not Applicable
Recruiting
Conditions
Parkinson's Disease, Essential Tremor
Registration Number
DRKS00032470
Lead Sponsor
niversität zu Köln, Zentrum für Klinische Studien Köln
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
45
Inclusion Criteria

Uni- or bilateral implantation of DBS leads in the subthalamic nucleus (PD) or the ventral intermedius nucleus of the thalamus and the posterior subthalamic area (ET) at least 3 months prior to study inclusion and confirmed diagnosis of Parkinson's Disease or Essential Tremor.
Patients with Parkinson’s Disease must have a relevant tremor burden defined as = 2 of 4 points of the MDS-UPDRS item 3.17 (rest tremor) without medication, patients with Essential Tremor =2 of 4 points of item 5/6 of the Fahn Tolosa Marin Tremor Rating Scale (postural or intention tremor).
Patients must be able to consent to participate at the study and to give written informed consent prior to study inclusion.

Exclusion Criteria

Non-fulfillment of all inclusion criteria

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Difference in tremor suppression, assessed by accelerometry, with energy-equivalent stimulation using two different stimulation frequencies (130 Hz vs 185 Hz)
Secondary Outcome Measures
NameTimeMethod
-Amplitude-equivalent effects of the different frequencies on tremor<br>- effects on therapeutic window<br>- for PD, effects on rigidity and bradykinesia
© Copyright 2025. All Rights Reserved by MedPath