Thoracic Spinal Cord Stimulation as a Symptomatic Treatment for Advanced Parkinson's Disease

Assistance Publique - Hôpitaux de Paris6 enrolled

Overview

Following the so call "honey moon" period, motor symptoms of Parkinson's Disease (PD) become difficult to control with dopaminergic treatments alone. Deep brain stimulation (DBS) of the subthalamic nucleus and internal globus pallidus helps to treat fluctuating parkinsonian patients restoring a decent quality of life. However, DBS need a long, complex and invasive surgery to succeed. Thus, there is a critical need to develop alternative treatments, more accessible and less invasive. Thoracic posterior spinal cord stimulation has been used for decades to treat chronic neuropathic pains. Safety and efficacy have already been demonstrated in neuropathic pain. Experimentally, SCS has also demonstrated to improve locomotor activity in two different rodents' models of parkinson's disease. The purpose of this study is to determine whether thoracic SCS is safe and could induce a benefit motor parkinsonian symptoms without any impact on cognitive function and axial disability.

The present pilot study will enroll 6 patients suffering from advanced Parkinson Disease (PD). Investigator will assess the safety, tolerance and efficacy of Spinal Cord Stimulation (SCS) with frequencies of 50, 100 and 130 Hz in a shuffle randomized for each patient. Briefly, each frequency will be evaluated immediately after and 4 weeks following SCS initiation with UPDRS-III, pain scales, and Hauser's diary. The best frequency for each patient will be then selected and maintained activated for 12 additional weeks. At the end of these 12 weeks, new assessment including UPDRS, visual pain scale, "SAINT-ANTOINE" Pain Questionary, PDQ-39 (quality of life), daily L-dopa equivalent dose, MDRS (cognitive status), LARS (apathy status) and MADRS (depression status) will be compared to the inclusion data of each patient. Primary endpoints include the safety of thoracic SCS by collected the number of adverse event and the efficacy by measuring the UPDRS-III OFF med/ON stim at 30 weeks.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Eligibility

Sex: ALLMin age: 45 YearsMax age: 69 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient from 45 to 69 years old * Affiliated to the French social health care system * Menopausal or under contraception for women * Parkinson's disease according to UK PDSBB's criteria with diagnosis for ≥ 5 years * OFF UPDRS-III ≥ 25 * Acute dopa-response ≥ 50% for UPDRS-III in an L-Dopa challenge * Fluctuations with periods off ≥ 25% of the time of awakening or dyskinesia ≥ 25% * 3≤ Hoehn \& Yahr ≤ 4 * No change in anti-parkinsonian drugs in the last month * Informed consent signed for the study Exclusion Criteria: * Patients major protected * Pregnancy * Deep brain stimulation or other neurosurgical treatment * MDRS Score \< 130 or depression scale MADRS ≥ 20 * Respiratory insufficiency (surgery belly decubitus) * Abnormalities on brain MRI which evoke a secondary parkinsonian syndrome * Spinal cord's injury on MRI or posterior cordonal's pathology on sensitive evoked potential * Neuropathy on EMG * Prior spinal surgery and spinal pathology at the dorsal level * Patients having already been included in therapeutic studies * Patient with a cardiac pacemaker, a defibrillator or any other implanted active pacemaker * Patient requiring diathermy process * Patient having a pathology requiring an MRI follow-up care

Outcomes

Primary Outcomes

Number of severe adverse events and adverse events reported

Time frame: at week 30

Secondary Outcomes

Tolerance and global statement

Clinical assessment

Time frame: After surgery (DO), at week 4, 8, 13, 18 and 30

Difference of UPDRS-III scores with and without stimulation in ON or OFF medication state

Time frame: At W4, W9, W14,W30

Difference of UPDRS-III scores without stimulation and after 4 weeks of continuous stimulation in ON or OFF medication state

Time frame: At W4, W8, W9, W13, W14,W18

Difference of global UPDRS between screening and others visits, in OFF and ON medication state

Time frame: At W-4, W8, W13, W18,W30

Difference of Walking Time Measurement scores with and without stimulation in ON or OFF medication state

Time frame: At W4, W9, W14,W30

Difference of Walking Time Measurement scores without stimulation and after 4 weeks of continuous stimulation in ON or OFF medication state

Time frame: At W4, W8, W9, W13, W14,W18

Pain assessment using visual pain scale and Saint Antoine Pain Questionnaire

Time frame: After 4, 9, 13 and 30 weeks after surgery

Paresthesia assessment using visual pain scale and Saint Antoine Pain Questionnaire

Time frame: After 4, 9, 13 and 30 weeks after surgery

Clinical abnormalities demonstrated during a comprehensive sensitive examination

Time frame: At W4, W8, W13, W18, W30

Differences of MDRS, LARS, MADRS, PDQ-39 scores between screening and the end of the study

Time frame: At W-4 and W30

Change of daily L-Dopa equivalent dose

Time frame: At W4, W8, W13, W18, W30

Thoracic Spinal Cord Stimulation as a Symptomatic Treatment for Advanced Parkinson's Disease

Overview

Conditions

Interventions

Eligibility

Locations (1)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts