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Clinical Trials/NCT03496532
NCT03496532
Withdrawn
Not Applicable

Optimization of Parameters of Subthalamic Nucleus Stimulation

Colette Boex1 site in 1 countryOctober 10, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
Colette Boex
Locations
1
Primary Endpoint
Comparison of quantity of Beta oscillations after pseudo random (Poisson distribution) vs uniform distribution of pulse time intervals
Status
Withdrawn
Last Updated
4 years ago

Overview

Brief Summary

Deep brain stimulation of the subthalamic nucleus is an effective treatment for Parkinson's disease. The analysis of cerebral signals of the subthalamic nucleus by local field potentials, provides one of the main electrophysiological markers of the success of the stimulation. This marker can be used to evaluate new paradigms of stimulation. So far, little studied, the temporal characteristics of the stimulation are very important in the effectiveness of the stimulation of the subthalamic nucleus, in Parkinson's disease. The first objective (Study I) is to compare the effectiveness of the stimulation when it is applied with biphasic symmetrical pulses and when applied with the standard pulses applied so far.

The second objective (Study II) is to see if, by applying pseudo-random time intervals between each stimulation pulse, if it would be possible to improve the efficiency and to limit the side effects of the stimulation.

The third objective (Study III) is to evaluate the electrophysiological changes of the subthalamic nucleus caused by the general anesthesia, in the anticipation of the realization of the surgery of the stimulation of the subthalamic nucleus under general anesthesia.

Detailed Description

Study I and II: Patients who participate undergo pulse generator change under sedation. Four sets of stimulation parameters will be compared. The efficacy of every set will be measured on induced changes in LFP recorded from the STN electrodes. LFP will be compared between before, during and right after each stimulation conditions. The stimulation order will be randomized. All other stimulation parameters will be the same (macrocontact with most beta-oscillations, 1 minute, 1.5mA) . Study III: Patients who participate undergo their first pulse generator implantation, performed under general anesthesia because of wire tunnelisation. The depth of anesthesia will be documented, recording the BIS spectral analysis index. The difference in spectral amplitude density of LFP, in particular in beta band oscillations will be correlated with the depth of anesthesia as measured with the BIS index at the time of 2 minutes recordings.

Registry
clinicaltrials.gov
Start Date
October 10, 2018
End Date
May 3, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Sequential
Sex
All

Investigators

Sponsor
Colette Boex
Responsible Party
Sponsor Investigator
Principal Investigator

Colette Boex

Principal investigator

University Hospital, Geneva

Eligibility Criteria

Inclusion Criteria

  • patients suffering from Parkinson's disease, who must undergo surgery for the replacement of their neurostimulator (under sedation) or for the first positioning of it
  • capacity of discernment
  • informed signed consent

Exclusion Criteria

  • Health considerations in regard to adding 13' in surgery room (e.g. pain or incomfort).

Outcomes

Primary Outcomes

Comparison of quantity of Beta oscillations after pseudo random (Poisson distribution) vs uniform distribution of pulse time intervals

Time Frame: 10 minutes per patient

% of changes in the energy of Beta oscillations

Comparison of quantity of Beta oscillations after biphasic pulses vs standard monophasic pulses

Time Frame: 10 minutes per patient

% of changes in the energy of Beta oscillations

Observe the evolution of Beta oscillations during deep anesthesia

Time Frame: 2 minutes per patient

Energy of Beta oscillations

Study Sites (1)

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