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A Novel Non Invasive Brain Stimulation Based Treatment for Chronic Low Back Pain (CLBP)

Primary Purpose

Chronic Low Back Pain

Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Neuroelectrics STARSTIM
Sponsored by
Tel-Aviv Sourasky Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Low Back Pain

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. age 18 to 70
  2. CLBP as defined by the European guidelines

Exclusion Criteria:

  1. Acute low back pain (duration of less than 6 months
  2. Neurological illness causing structural brain damage (e.g. Stroke, TIA)
  3. Psychiatric disease other than mood disorders
  4. Current chronic use of medications with pro-epileptic properties
  5. Known alcohol dependency
  6. Use of alcohol within the previous 24 hours
  7. History of loss of consciousness
  8. Epilepsy or epilepsy in a first degree relative
  9. Medical implants
  10. Pregnancy
  11. Illicit drug use or within the previous month

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    NIBS tDCS/tACS stimulation

    inactive electrodes

    Arm Description

    Each patient will undergo initial diagnosis with NIBS algorithm utilizing EEG measurements combined with TMS. Initial diagnosis will last 10 minutes in which EEG measurement will be recorded 5 minutes and then in combination with TMS for another 5 minutes with no more than 500 TMS stimuli applied to cortex at low frequency of up to 5Hz. EEG recording will be analyzed by NIBS algorithm which will propose a course of treatment with the following limitations: stimulation of 2mA (32, 33) current after 30 seconds ramp up of 0.1mA increments, 20 min for each session, twice a week

    diagnosis and monitoring will be performed as in active treatment, but during treatment anodal/cathodal/alternate stimulation will begin and automatically stop after 30 seconds leaving subject with an inactive electrodes in place for the remainder of treatment duration

    Outcomes

    Primary Outcome Measures

    Evaluation of treatment efficacy (evaluated by pain level and sleep quality questionnaire)
    Efficacy of the treatment will be evaluated by pain level and sleep quality questionnaire

    Secondary Outcome Measures

    Full Information

    First Posted
    March 8, 2015
    Last Updated
    March 18, 2015
    Sponsor
    Tel-Aviv Sourasky Medical Center
    Collaborators
    NIBS NeuroScience Technologies
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02393391
    Brief Title
    A Novel Non Invasive Brain Stimulation Based Treatment for Chronic Low Back Pain (CLBP)
    Official Title
    Novel Non Invasive Brain Stimulation Based Treatment for Chronic Low Back
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    May 2015 (undefined)
    Primary Completion Date
    May 2015 (Anticipated)
    Study Completion Date
    undefined (undefined)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Tel-Aviv Sourasky Medical Center
    Collaborators
    NIBS NeuroScience Technologies

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Neuropathic pain results from damage to or dysfunction of the peripheral or central nervous system, rather than stimulation of pain receptors. Diagnosis is suggested by pain out of proportion to tissue injury, dysesthesia (eg, burning, tingling), and signs of nerve injury detected during neurologic examination. Although neuropathic pain responds to opioids, treatment is often with adjuvant drugs (eg, antidepressants, anticonvulsants, baclofen, topical drugs). Neuropathic pain (e.g. phantom limb pain, CRPS, postherpetic neuralgia, postsurgical pain syndromes, CLBP etc.) remains a challenging condition to treat because it is commonly refractory to classical pharmacological and to surgical treatment approaches. Chronic low back pain (CLBP) is a widespread and costly problem for which few interventions are effective. An increased focus on the study of the nervous system and its involvement in pain disorders has documented complex neuronal activity and structural changes at a peripheral, as well as at spinal cord and cortical levels indicating a neuropathic element in CLBP. Accumulated evidence suggests that neuropathic pain in general and CLBP specifically might be associated to brain cortical plastic changes. Thus an ideal rehabilitative approach should aim to reverse them. In line with this idea, the investigators suggest an innovative noninvasive intervention aimed at alleviating neuropathic pain. New rehabilitative approaches have been proposed to try and reverse this cortical reorganization. Results of several studies have shown that motor cortex stimulation with epidural electrodes or repetitive transcranial magnetic stimulation (rTMS) or transcranial direct stimulation (tDCS) are effective in reducing pain in patients with central pain refractory to treatment. Transcranial direct current stimulation (tDCS) is an easily applied and safe technique by which brain activity can be modulated noninvasively and can decrease pain in patients with refractory central pain. The investigators hypothesized that focal-tDCS treatment personally customized to each patients basal neuronal network properties would result in both acute and long term pain relief for neuropathic pain patients.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Low Back Pain

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    80 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    NIBS tDCS/tACS stimulation
    Arm Type
    Active Comparator
    Arm Description
    Each patient will undergo initial diagnosis with NIBS algorithm utilizing EEG measurements combined with TMS. Initial diagnosis will last 10 minutes in which EEG measurement will be recorded 5 minutes and then in combination with TMS for another 5 minutes with no more than 500 TMS stimuli applied to cortex at low frequency of up to 5Hz. EEG recording will be analyzed by NIBS algorithm which will propose a course of treatment with the following limitations: stimulation of 2mA (32, 33) current after 30 seconds ramp up of 0.1mA increments, 20 min for each session, twice a week
    Arm Title
    inactive electrodes
    Arm Type
    Placebo Comparator
    Arm Description
    diagnosis and monitoring will be performed as in active treatment, but during treatment anodal/cathodal/alternate stimulation will begin and automatically stop after 30 seconds leaving subject with an inactive electrodes in place for the remainder of treatment duration
    Intervention Type
    Device
    Intervention Name(s)
    Neuroelectrics STARSTIM
    Primary Outcome Measure Information:
    Title
    Evaluation of treatment efficacy (evaluated by pain level and sleep quality questionnaire)
    Description
    Efficacy of the treatment will be evaluated by pain level and sleep quality questionnaire
    Time Frame
    one year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: age 18 to 70 CLBP as defined by the European guidelines Exclusion Criteria: Acute low back pain (duration of less than 6 months Neurological illness causing structural brain damage (e.g. Stroke, TIA) Psychiatric disease other than mood disorders Current chronic use of medications with pro-epileptic properties Known alcohol dependency Use of alcohol within the previous 24 hours History of loss of consciousness Epilepsy or epilepsy in a first degree relative Medical implants Pregnancy Illicit drug use or within the previous month
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Silviu Brill, Dr.
    Phone
    97236974581
    Email
    paincenter@tlvmc.gov.il

    12. IPD Sharing Statement

    Learn more about this trial

    A Novel Non Invasive Brain Stimulation Based Treatment for Chronic Low Back Pain (CLBP)

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