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Asia Coma Electrical Stimulation (the ACES Trial) (ACES)

Primary Purpose

TBI (Traumatic Brain Injury)

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Right median nerve stimulation
Sponsored by
RenJi Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for TBI (Traumatic Brain Injury) focused on measuring Coma, traumatic brain injury, median nerve stimulation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A confirmed history of closed traumatic brain injury 10 days before enrollment
  • A Glasgow coma scale (GCS) score of 4-8 or the motor part less than 5 if the patient received tracheotomy.
  • 18-65 years of age

Exclusion Criteria:

  • Unstable vital signs
  • Have a history of severe cardiac arrhythmias, implanted pacemaker, as well as seizures
  • Pregnancy
  • No informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    No Intervention

    Arm Label

    RMNS group

    Control group

    Arm Description

    Focus intervention: right median nerve stimulation plus standard management

    Standard management

    Outcomes

    Primary Outcome Measures

    Proportion of patients returning consciousness
    The term "consciousness" is defined when the patient shows objective ability to respond to verbal commands.

    Secondary Outcome Measures

    Duration of unconsciousness
    This outcome is defined as the time between trauma and objective recovery of the ability to respond to verbal commands
    Adverse events
    The potential adverse events include but not limited to seizures, intracranial bleeding, increased sympathetic activity and so on.
    Glasgow Coma Scale (GCS)
    Coma Recovery Scale-Revised (CRS-R)
    Disability Rating Scale (DRS)
    Full Outline of UnResponsiveness scale(FOUR)

    Full Information

    First Posted
    December 23, 2015
    Last Updated
    December 31, 2015
    Sponsor
    RenJi Hospital
    Collaborators
    All India Institute of Medical Sciences, New Delhi, JSC National Center for Neurosurgery, Republic of Kazakhstan, College of Medical Sciences Teaching Hospital. Nepal
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02645578
    Brief Title
    Asia Coma Electrical Stimulation (the ACES Trial)
    Acronym
    ACES
    Official Title
    Asia Coma Electrical Stimulation Trial: an Asian Multicenter Randomized Controlled Trial to Assess the Efficacy and Safety of Right Median Nerve Stimulation for Traumatic Coma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    January 2016 (undefined)
    Primary Completion Date
    June 2017 (Anticipated)
    Study Completion Date
    December 2017 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    RenJi Hospital
    Collaborators
    All India Institute of Medical Sciences, New Delhi, JSC National Center for Neurosurgery, Republic of Kazakhstan, College of Medical Sciences Teaching Hospital. Nepal

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    This study is a prospective multicenter randomized controlled trial from Asian countries to compare the effect and safety of right median nerve stimulation versus traditional treatment for comatose patients at the early stage following traumatic brain injury.
    Detailed Description
    Traumatic brain injury (TBI) is a leading cause of mortality and morbidity and one of the greatest unmet needs in public health. The most severe injury can lead to a poor outcome and prolonged coma of the victims. It is estimated that ten to fifteen percent of the severe TBI patients are discharged in a prolonged coma or a vegetative state. However, no treatment measure to data has been proven robustly to alter the pace of recovery or improve neurological outcome of the comatose patients following TBI. Although right median nerve electrical stimulation (RMNS) has been used clinically for more than two decades, no strong evidence of efficacy was generated because of the limitations in the past trials including a small sample size or the inappropriate study design. In the present study, a multicenter research network with inclusion of neurotrauma centers from China, India, Nepal and Kazakhstan was established with the aim to validate the efficacy and safety of a promising intervention strategy for traumatic coma at early stage. Since RMNS is a simple, inexpensive, noninvasive technique with a good safety profile, our study will probably add more evidence to the treatment of traumatic coma in Asian countries.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    TBI (Traumatic Brain Injury)
    Keywords
    Coma, traumatic brain injury, median nerve stimulation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    360 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    RMNS group
    Arm Type
    Experimental
    Arm Description
    Focus intervention: right median nerve stimulation plus standard management
    Arm Title
    Control group
    Arm Type
    No Intervention
    Arm Description
    Standard management
    Intervention Type
    Device
    Intervention Name(s)
    Right median nerve stimulation
    Other Intervention Name(s)
    RMNS
    Intervention Description
    Right median nerve electrical stimulation (RMNS) is administered via a pair of lubricated one-inch square rubber surface electrodes pasted on the volar aspect of the right distal forearm over the median nerve. An electrical neuromuscular stimulator supplied trains of asymmetric biphasic pluses at an amplitude of 20 milliamps with a pulse width of 300 microseconds at 40 Hz for 20 sec/min. The RMNS treatment continues 8 hours per day for two weeks.
    Primary Outcome Measure Information:
    Title
    Proportion of patients returning consciousness
    Description
    The term "consciousness" is defined when the patient shows objective ability to respond to verbal commands.
    Time Frame
    Within six months after injury
    Secondary Outcome Measure Information:
    Title
    Duration of unconsciousness
    Description
    This outcome is defined as the time between trauma and objective recovery of the ability to respond to verbal commands
    Time Frame
    Within six months after injury
    Title
    Adverse events
    Description
    The potential adverse events include but not limited to seizures, intracranial bleeding, increased sympathetic activity and so on.
    Time Frame
    Within six months post injury
    Title
    Glasgow Coma Scale (GCS)
    Time Frame
    28 days post injury
    Title
    Coma Recovery Scale-Revised (CRS-R)
    Time Frame
    six months post injury
    Title
    Disability Rating Scale (DRS)
    Time Frame
    six months post injury
    Title
    Full Outline of UnResponsiveness scale(FOUR)
    Time Frame
    28 days post injury

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: A confirmed history of closed traumatic brain injury 10 days before enrollment A Glasgow coma scale (GCS) score of 4-8 or the motor part less than 5 if the patient received tracheotomy. 18-65 years of age Exclusion Criteria: Unstable vital signs Have a history of severe cardiac arrhythmias, implanted pacemaker, as well as seizures Pregnancy No informed consent
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Guoyi Gao
    Email
    guoyigao@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Jin Lei
    Email
    smiles1949@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jiyao Jiang
    Organizational Affiliation
    RenJi Hospital
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Junfeng Feng
    Organizational Affiliation
    RenJi Hospital
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Guoyi Gao
    Organizational Affiliation
    RenJi Hospital
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    Yes
    Citations:
    PubMed Identifier
    25664378
    Citation
    Lei J, Wang L, Gao G, Cooper E, Jiang J. Right Median Nerve Electrical Stimulation for Acute Traumatic Coma Patients. J Neurotrauma. 2015 Oct 15;32(20):1584-9. doi: 10.1089/neu.2014.3768. Epub 2015 May 7.
    Results Reference
    background
    PubMed Identifier
    16350980
    Citation
    Cooper EB, Scherder EJ, Cooper JB. Electrical treatment of reduced consciousness: experience with coma and Alzheimer's disease. Neuropsychol Rehabil. 2005 Jul-Sep;15(3-4):389-405. doi: 10.1080/09602010443000317.
    Results Reference
    background
    PubMed Identifier
    14518515
    Citation
    Liu JT, Wang CH, Chou IC, Sun SS, Koa CH, Cooper E. Regaining consciousness for prolonged comatose patients with right median nerve stimulation. Acta Neurochir Suppl. 2003;87:11-4. doi: 10.1007/978-3-7091-6081-7_3.
    Results Reference
    background
    PubMed Identifier
    14518514
    Citation
    Cooper EB, Cooper JB. Electrical treatment of coma via the median nerve. Acta Neurochir Suppl. 2003;87:7-10. doi: 10.1007/978-3-7091-6081-7_2.
    Results Reference
    background
    PubMed Identifier
    11595086
    Citation
    Peri CV, Shaffrey ME, Farace E, Cooper E, Alves WM, Cooper JB, Young JS, Jane JA. Pilot study of electrical stimulation on median nerve in comatose severe brain injured patients: 3-month outcome. Brain Inj. 2001 Oct;15(10):903-10. doi: 10.1080/02699050110065709.
    Results Reference
    background
    PubMed Identifier
    28693604
    Citation
    Wu X, Zhang C, Feng J, Mao Q, Gao G, Jiang J. Right median nerve electrical stimulation for acute traumatic coma (the Asia Coma Electrical Stimulation trial): study protocol for a randomised controlled trial. Trials. 2017 Jul 10;18(1):311. doi: 10.1186/s13063-017-2045-x.
    Results Reference
    derived

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    Asia Coma Electrical Stimulation (the ACES Trial)

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