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
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
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
NCT ID
NCT02645578
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
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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