Effects of Stimulation Patterns of Deep Brain Stimulation

Enrolling by invitationNot a drug-phase studyMS (type not specified)NCT02553525

What it found

Still running

No result yet.

What was tested

Treatment tested

  • Therapeutic Stimulation Patterns
  • Symptogenic Stimulation Patterns

What it measured

Main measures

  • Tremor Accelerometry

    Day 1

    Physical function
  • Bradykinesia Finger Tapping

    Day 1

    Physical function
  • Neural Activity

    Day 1

    Myelin repairPhysical function

Other measures (1)

  • Electrode Location

    Day 1

Who could take part

MS (type not specified) · 21 to 80

Show the full criteria

Inclusion criteria

* Diagnosis of Parkinson's Disease (PD), Essential Tremor (ET) dystonia or Multiple Sclerosis (MS) * Scheduled to undergo Deep Brain Stimulation (DBS) electrode implant, IPG implant or implanted pulse generator (IPG) replacement surgery * Neurologically stable * Able to understand the study and consent form

Exclusion criteria

* Inability to execute the motor tasks during the study * Inability to tolerate withholding anti-parkinsonian and/or anti-tremor medications * Clinically ineffective DBS

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The purpose of this study is to measure the effects of non-regular temporal patterns of deep brain stimulation (DBS) on motor symptoms and neural activity in persons with Parkinson's disease (PD), essential tremor (ET), dystonia or multiple sclerosis (MS). These data will guide the design of novel stimulation patterns that may lead to more effective and reliable treatment with DBS. These data will also enable evaluation of current hypotheses on the mechanisms of action of DBS. Improving our understanding of the mechanisms of action of DBS may lead to full development of DBS as a treatment for Parkinson's disease and may lead to future applications of DBS.

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History

    1. Started

      Jun 2016

    2. Main results due

      Mar 2027

    3. Finished

      Mar 2027

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