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临床试验/NCT05148468
NCT05148468终止不适用

Effects of Spinal Cord Stimulation on Gait in Patients With Parkinson´s Disease; a Randomized, Crossover, Double Blinded, Placebo-Controlled Study

University of Sao Paulo General Hospital2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2021年11月30日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
8
试验地点
2
主要终点
Change on Timed Up and Go - Test 3 Meters (TUG-Test 3M)

研究概览

简要总结

Spinal cord stimulation (SCS) for Parkinson´s disease (PD) has been studied for a decade but consensus on efficacy is still lacking, with the previous stimulation standard paresthesia inducing threshold hampering adequate subject blinding. Considering that tonic stimulation for pain has been shown to be efficacious for most patients on subthreshold stimulation parameters we hypothesize a similar result with it´s use on PD. The investigators aim to:

  1. Produce stronger evidence on SCS efficacy for PD in regards to gait, motor scores and quality of life measures by incorporating subthreshold in a randomized cross over placebo-controlled study with a large sample.
  2. Identify predictors of good response to SCS therapy by performing trans spinal magnetic stimulation (TSMS) before SCS implant and correlating the response to SCS to that of the noninvasive TSMS.
  3. Better provide biomarkers of SCS therapy through functional magnetic resonance imaging and electroencephalographic mapping.

详细描述

Gait impairment in Parkinson´s Disease (PD) is often refractory to standard medication therapy and functional surgery options currently explored resulting in grave loss of independence and quality of life. Spinal cord stimulation (SCS) has been explored for its role in PD after enthusiastic animal studies and despite mixed initial results is currently a very promising candidate for ameliorating hard to treat gait and balance disorders.

Consensus on tonic SCS efficacy is hampered mostly due to small samples and lack of randomized controlled trials so far, and the impossibility of subject blinding due to standard stimulation settings using currents over the paresthesia inducing threshold. Some small studies already attempted subthreshold blinding and all resulted in non significant results, however with no important difference when switching to suprathreshold settings, thus raising the possibility of non responder subjects or inefficient therapy and calling for additional exploration. The investigators aim to explore the feasibility of a placebo controlled trial using subthreshold stimulation with a larger sample and produce stronger evidence on SCS efficacy for PD.

Additionally, the possibility of non responder subjects will be explored by correlating the degree of response to SCS to patient demographic characteristics including age, PD severity and cognition, gait characteristics and the degree of response to trans spinal magnetic stimulation (TSMS), a non invasive magnetic stimulation of upper thoracic spinal region, aiming to identify prognostic factors for the therapy.

Finally, functional magnetic resonance imaging and electroencephalographic mapping will be performed in order to identify biomarkers of SCS therapy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

Patients and examiners will be blinded to stimulation status

入排标准

年龄范围
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosed Parkinson´s Disease with Hoehn Yahr scale between 2,5 and 4,0
  • Main complaint of balance or freezing of gait
  • Score of 2 or more on subitem 3.11 of the MDS UPDRS scale concerning Freezing of Gait severity.
  • Capable of informed consent

排除标准

  • Frequent lower limb, lower back or hip pain scoring 3 or more on visual analog scale
  • Uncontrolled or serious comorbidities such as uncontrolled diabetes mellitus, renal disease, anticoagulation, immunosuppression or other medical conditions that present a contraindication for SCS surgery
  • Psychosis, uncontrolled depression (BDI >14) or anxiety disorder (BAI >14)

结局指标

主要结局

Change on Timed Up and Go - Test 3 Meters (TUG-Test 3M)

时间窗: 6 months

Comparison of the change in Timed Up and Go test times between ON-stimulation and baseline and sham-stimulation and baseline in double blinded setting.

次要结局

  • Unified Parkinson's Disease Rating Scale (MDS-UPDRS) - Part III(6 months)
  • Parkinson's Disease Questionnaire (PDQ39)(6 months)
  • New Freezing of Gait Questionnaire (NFOG-Q)(6 months)
  • 2 minute walk test(6 months)
  • Mini Balance Evaluation Systems Test (Mini-BESTest)(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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