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Clinical Trials/NCT04682678
NCT04682678
Completed
Not Applicable

Spinal Cord Stimulation for Gait Disorders in Parkinson's Disease: a Pilot Study

University Hospital, Grenoble1 site in 1 country6 target enrollmentMarch 10, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Parkinson Disease
Sponsor
University Hospital, Grenoble
Enrollment
6
Locations
1
Primary Endpoint
frequency and duration of Freezing Of Gait (FOG) episodes, objective
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Our project is based on the fundamental hypothesis that epidural spinal cord stimulation (SCS) improves Freezing of gait (FOG) in patients with Parkinson's disease. In eight patients implantation of electrodes for SCS at the epidural thoracic level will be performed under general anaesthesia.

Evaluation of gait and motor symptoms will be performed with and without stimulation, after a 3-month period for each of the stimulation conditions.This is a pilot, single centre, prospective, randomized, double blinded, cross-over study.

Detailed Description

Patients will be selected in the Movement Disorders Unit, Department of Neurology, University Hospital Grenoble. A preoperative assessment with gait assessment, clinical evaluation and Non-Motor Symptoms assessment will be realized. The implantation of electrodes for SCS at the epidural thoracic level connected to a neurostimulator at the abdominal level will be performed under general anaesthesia. During the first postoperative month, the optimization of SCS parameters will be performed by an experienced movement disorders neurologist.After the first post-operative month the patient will be randomized to the STIM ON condition (stimulation on, with the most effective parameters) or STIM OFF (without stimulation). The randomization will be performed in a double blinded fashion, by a neurologist working in open and not participating in the evaluations. After 3 months, the patient will be evaluated in a double blind condition, and the stimulation condition will be crossed for another period of 3 months. At the end of this second 3-month period, the patient will be again double-blind assessed. After this evaluation, the patient will enter the open phase of the study for a period of 6 months. For this last phase of the study, under STIM ON condition, an optimization of the stimulation settings will be realized, if necessary. At the end of this 6-month period of stimulation, the patient will be evaluated one last time. At all visits, clinical and gait evaluations will be carried out under chronic dopaminergic treatment. No change in antiparkinsonian treatment will be allowed during the entire study. Gait and clinical assessment will be performed at baseline and at the end of each double blinded phase and at 1-year follow-up. For the double-blind study the patient, the neurologist who performs the clinical evaluation and the expert who performs the gait test and analysis will be blind to the stimulation condition.

Registry
clinicaltrials.gov
Start Date
March 10, 2021
End Date
July 11, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
University Hospital, Grenoble
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

frequency and duration of Freezing Of Gait (FOG) episodes, objective

Time Frame: Month 6

gait testing

Secondary Outcomes

  • impact of spinal cord stimulation on FOG, long term outcome(Month 12)
  • impact of spinal cord stimulation on quality of life, long term outcome(Month 12)
  • impact of SCS on gait during a dual cognitive-motor task test(Month 12)
  • impact of SCS on gait during timed up and go test(Month 12)
  • frequency and duration of Freezing Of Gait (FOG) episodes, subjective 2(Month 12)
  • frequency and duration of Freezing Of Gait (FOG) episodes, subjective 1(Month 12)
  • impact of SCS on other non-motor symptoms(Month 12)

Study Sites (1)

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