Spinal cord stimulation therapy for patients with Parkinson's disease and gait problems (STEP-PD): study protocol for an exploratory, double-blind, randomised, placebo-controlled feasibility trial

被引:2
|
作者
Hvingelby, Victor S. [1 ,2 ]
Terkelsen, Miriam Hojholt [1 ,2 ]
Johnsen, Erik L. [3 ,4 ]
Moller, Mette [4 ]
Danielsen, Erik Hvid [4 ]
Henriksen, Tove [5 ]
Glud, Andreas Norgaard [3 ,6 ]
Tai, Yen [7 ]
Andersen, Anne Sofie Moller [6 ]
Meier, Kaare [3 ,6 ]
Borghammer, Per [3 ,8 ,9 ]
Moro, Elena [10 ]
Sorensen, Jens Christian Hedemann [3 ,6 ]
Pavese, Nicola [1 ,2 ]
机构
[1] Aarhus Univ, Dept Clin Med Nucl Med, Aarhus, Denmark
[2] Aarhus Univ, PET Ctr, Aarhus, Denmark
[3] Aarhus Univ, Dept Clin Med, Aarhus, Denmark
[4] Aarhus Univ Hosp, Dept Neurol, Aarhus, Denmark
[5] Bispebjerg Hosp, Dept Neurol, Copenhagen, Denmark
[6] Aarhus Univ Hosp, Dept Neurosurg, Aarhus, Denmark
[7] Imperial Coll Healthcare NHS Trust, Dept Neurosci, London, England
[8] Aarhus Univ Hosp, Dept Nucl Med, Aarhus, Denmark
[9] Aarhus Univ Hosp, PET Ctr, Aarhus, Denmark
[10] Grenoble Alpes Univ Hosp, Dept Psychiat Neurol Neurol Rehabil & Forens Med, Grenoble, Auvergne Rhone, France
关键词
PEDUNCULOPONTINE;
D O I
10.1136/bmjno-2022-000333
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Gait difficulties are common in Parkinson's disease (PD) and cause significant disability. These symptoms are often resistant to treatment. Spinal cord stimulation (SCS) has been found to improve gait, including freezing of gait, in a small number of patients with PD. The mechanism of action is unclear, and some patients are non-responders. With this double-blind, placebo-controlled efficacy and feasibility clinical and imaging study, we aim to shed light on the mechanism of action of SCS and collect data to inform development of a scientifically sound clinical trial protocol. We also aim to identify clinical and imaging biomarkers at baseline that could be predictive of a favourable or a negative outcome of SCS and improve patient selection. Methods and analysis A total of 14 patients will be assessed with clinical rating scales and gait evaluations at baseline, and at 6 and 12 months after SCS implantation. They will also receive serial F-18-deoxyglucose and (FEOBV)-F-18 PET scans to assess the effects of SCS on cortical/subcortical activity and brain cholinergic function. The first two patients will be included in an open pilot study while the rest will be randomised to receive active treatment or placebo (no stimulation) for 6 months. From this point, the entire cohort will enter an open label active treatment phase for a subsequent 6 months. Ethics and dissemination This study was reviewed and approved by the Committee on Health Research Ethics, Central Denmark RM. It is funded by the Danish Council for Independent Research. Independent of outcome, the results will be published in peer-reviewed journals and presented at national and international conferences.
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页数:7
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