Motor Threshold and Motor Cortex Stimulation
Primary Purpose
Neuropathic Pain
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Change of PMT setting
Sponsored by
About this trial
This is an interventional treatment trial for Neuropathic Pain focused on measuring motor cortex stimulation, chronic neuropathic pain
Eligibility Criteria
Inclusion Criteria:
- Adult patient more than 18 years of age
- Chronic neuropathic pain effectively treated with motor cortex stimulation
- Stable medication during the trial
- Willing and able to comply with the study protocol and to return per the follow-up visit schedule and able to provide informed consent.
Exclusion Criteria:
- Evidence of an active disruptive psychiatric disorder or other known condition significant enough to impact the perception of pain, compliance to intervention and/or ability to evaluate treatment outcome as determined by the investigator
- Technical malfunction of the MCS device
- History of seizures
- Unable to provide informed consent
Sites / Locations
- Vancouver General Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Experimental
Arm Label
-10% of effective PMT
former setting (+/- 0% of PMT)
+10% of effective PMT
Arm Description
Patients are set to a voltage 10% less than their original PMT at start of study, Changes in PMT settings
Patients are set to their original PMT at start of study, Changes in PMT settings
Patients are set to a voltage 10% more than their original PMT at start of study, Changes in PMT settings
Outcomes
Primary Outcome Measures
Change in Pain measured on the Visual Analogue Scale with different PMT Settings
Secondary Outcome Measures
Quality of Life assessment with the SF-36 questionnaire
Full Information
NCT ID
NCT02255643
First Posted
September 25, 2014
Last Updated
December 16, 2014
Sponsor
University of British Columbia
1. Study Identification
Unique Protocol Identification Number
NCT02255643
Brief Title
Motor Threshold and Motor Cortex Stimulation
Official Title
The Relationship Between Motor Threshold and Effective Stimulation Threshold During Motor Cortex Stimulation
Study Type
Interventional
2. Study Status
Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
October 2014 (undefined)
Primary Completion Date
November 2014 (Actual)
Study Completion Date
December 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of British Columbia
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Motor cortex stimulation (MCS) is a form of brain stimulation for patients with neuropathic pain not responsive to medication. An electrode is placed on the surface of the brain and connected to a programmable battery in the chest.
The strength of stimulation can be individually adjusted by changing the voltage of stimulation. A too high voltage will produce side effects (e.g. seizures) while a too low voltage will not provide pain control. The aim of this study is to analyze the optimal stimulation parameters in patients already implanted with a motor cortex stimulation who have received good pain relief. The actual voltage may vary widely between patients but the investigators feel that there may be an "ideal" voltage if it is measured as a percentage of motor threshold (PMT). If motor threshold is the stimulation voltage that can evoke a muscle contraction then a PMT = 80% would be a voltage that was eighty percent of that value. Although the actual voltage may be widely different between patients, the percentage needed may be very similar. The investigators therefore plan to measure the effect of different percentages of PMT in patients already being treated with motor cortex stimulation.
Systematic analysis of the findings of this study might help the individual participant and future patients to better programming and less side effects.
Detailed Description
Motor cortex stimulation (MCS) is a form of brain stimulation for patients with medically refractory neuropathic pain. The strength of stimulation can be individually adjusted by changing the voltage of stimulation. Too high voltage will produce side effects (e.g. seizures) while too low voltage will not provide pain control. The aim of this study is to analyze the optimal stimulation parameters in patients already implanted with a motor cortex stimulation who have received good pain relief. The actual voltage may vary widely between patients (because of the individual variations in tissue resistance) but the investigators feel that there may be an "ideal" voltage if it is measured as a percentage of motor threshold (PMT).
If motor threshold is the voltage that can evoke a muscle contraction then a PMT = 80% would be a voltage that was eighty percent of that value. Although the actual voltage may be different between patients, the effective PMT may be similar since it represents a more physiologic measure of stimulation.
Systematic analysis of the findings of this study might help the individual participant and future patients by reducing voltage to the lowest effective setting and reducing the chance of seizures.
Motor cortex stimulation is used in the treatment of neuropathic pain since 1991 but still no guidelines for programming exist and programming is therefore mainly bases on trial and error. This is mostly due to many variables influencing the choice of stimulation parameters and significant individual differences in susceptibility to stimulation. Routinely the motor threshold is determined during programming to identify the superior limit of voltage at which twitching is induced. No stimulation above the motor threshold should be performed as this is known to cause seizures. The voltage of simulation that will be effective for an individual is unknown at the beginning of the treatment.
The investigators try to find the lowest effective voltage because that will reduce the risk of stimulation-induced seizures and prolong the life of the pacemaker.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuropathic Pain
Keywords
motor cortex stimulation, chronic neuropathic pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Randomized
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
-10% of effective PMT
Arm Type
Experimental
Arm Description
Patients are set to a voltage 10% less than their original PMT at start of study, Changes in PMT settings
Arm Title
former setting (+/- 0% of PMT)
Arm Type
Active Comparator
Arm Description
Patients are set to their original PMT at start of study, Changes in PMT settings
Arm Title
+10% of effective PMT
Arm Type
Experimental
Arm Description
Patients are set to a voltage 10% more than their original PMT at start of study, Changes in PMT settings
Intervention Type
Device
Intervention Name(s)
Change of PMT setting
Intervention Description
The patients current motor threshold is determined and the patient is set to a new PMT (= new treatment arm)
Primary Outcome Measure Information:
Title
Change in Pain measured on the Visual Analogue Scale with different PMT Settings
Time Frame
at the End of each trial period, typically 14 days after changes in PMT Settings
Secondary Outcome Measure Information:
Title
Quality of Life assessment with the SF-36 questionnaire
Time Frame
at the end of each trial period, typically at 14 days
Other Pre-specified Outcome Measures:
Title
Pain assessment with the McGill pain questionnaire to record impact of pain
Time Frame
at the end of each trial period, typically 14 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patient more than 18 years of age
Chronic neuropathic pain effectively treated with motor cortex stimulation
Stable medication during the trial
Willing and able to comply with the study protocol and to return per the follow-up visit schedule and able to provide informed consent.
Exclusion Criteria:
Evidence of an active disruptive psychiatric disorder or other known condition significant enough to impact the perception of pain, compliance to intervention and/or ability to evaluate treatment outcome as determined by the investigator
Technical malfunction of the MCS device
History of seizures
Unable to provide informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher R Honey, MD, DPhil
Organizational Affiliation
UBC
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver General Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V5Z 4E3
Country
Canada
12. IPD Sharing Statement
Citations:
PubMed Identifier
1705329
Citation
Tsubokawa T, Katayama Y, Yamamoto T, Hirayama T, Koyama S. Treatment of thalamic pain by chronic motor cortex stimulation. Pacing Clin Electrophysiol. 1991 Jan;14(1):131-4. doi: 10.1111/j.1540-8159.1991.tb04058.x.
Results Reference
background
PubMed Identifier
1792954
Citation
Tsubokawa T, Katayama Y, Yamamoto T, Hirayama T, Koyama S. Chronic motor cortex stimulation for the treatment of central pain. Acta Neurochir Suppl (Wien). 1991;52:137-9. doi: 10.1007/978-3-7091-9160-6_37.
Results Reference
background
PubMed Identifier
8657427
Citation
Peyron R, Garcia-Larrea L, Deiber MP, Cinotti L, Convers P, Sindou M, Mauguiere F, Laurent B. Electrical stimulation of precentral cortical area in the treatment of central pain: electrophysiological and PET study. Pain. 1995 Sep;62(3):275-286. doi: 10.1016/0304-3959(94)00211-V.
Results Reference
background
PubMed Identifier
18541887
Citation
Lima MC, Fregni F. Motor cortex stimulation for chronic pain: systematic review and meta-analysis of the literature. Neurology. 2008 Jun 10;70(24):2329-37. doi: 10.1212/01.wnl.0000314649.38527.93.
Results Reference
background
Learn more about this trial
Motor Threshold and Motor Cortex Stimulation
We'll reach out to this number within 24 hrs