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Spinal Magnetic Stimulation in Neuropathic Pain

Primary Purpose

Neuropathic Pain

Status
Completed
Phase
Phase 3
Locations
Singapore
Study Type
Interventional
Intervention
magnetic stimulation
Magnetic Stimulation with tilted coil
Sponsored by
Singapore General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neuropathic Pain focused on measuring magnetic stimulation, neuropathic pain, spinal, lower limb, clinical trial

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All with neuropathic lower limb pain

Exclusion Criteria:

  • Contraindications to magnetic stimulation

Sites / Locations

  • Singapore General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Magnetic Stimulation

Magnetic Stimulation with tilted coil

Arm Description

Magnetic Stimulation with tilted coil

Outcomes

Primary Outcome Measures

Subjective pain score measurements
NAS score

Secondary Outcome Measures

Full Information

First Posted
March 4, 2007
Last Updated
March 30, 2010
Sponsor
Singapore General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00443469
Brief Title
Spinal Magnetic Stimulation in Neuropathic Pain
Official Title
A Randomized Placebo-controlled Trial on the Use of Repetitive Spinal Magnetic Stimulation as a Therapeutic Option in Patients With Intractable Neuropathic Pain of the Lower Limbs
Study Type
Interventional

2. Study Status

Record Verification Date
March 2010
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
February 2010 (Actual)
Study Completion Date
February 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Singapore General Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
It involves delivering a train of magnetic pulses, 5 at each time, to the brain. In the present study, we are using the same method to treat severe pain due to nerve conditions. You will be given up to 1000 pulses in total over the spine in the lower back (Spinal Magnetic Stimulation or SMS). Each train will be given in 10-second intervals. You will have SMS on a single day. You will be given SMS pulses at 1 or 10 per second. No stimulation will be given over the head. You will be assessed before and after the study for up to 1 week. Your usual medical treatment will be continued
Detailed Description
You must be aware of that this is a placebo-controlled trial. This means that you may either receive real SMS or sham SMS. The latter involves a harmless process of ineffective stimulation, designed for comparison with real SMS. Whether you receive either form of treatment will be assigned randomly, and there will be a 50% chance of being assigned to either.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neuropathic Pain
Keywords
magnetic stimulation, neuropathic pain, spinal, lower limb, clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Magnetic Stimulation
Arm Type
Experimental
Arm Title
Magnetic Stimulation with tilted coil
Arm Type
Placebo Comparator
Arm Description
Magnetic Stimulation with tilted coil
Intervention Type
Device
Intervention Name(s)
magnetic stimulation
Intervention Description
SMS was delivered with a repetitive magnetic stimulator connected to a figure of eight coil capable of delivering a maximum output of 2 Tesla per pulse. The coil measured 90 mm in each wing and was centered over the surface landmark corresponding to the cauda equina region. SMS was performed with the patient lying comfortably in the prone position and a soft pillow supported the lower abdomen. The coil was placed flat over the back with the handle pointing cranially. Each patient on active treatment received 200 trains of 5 pulses delivered at 10 Hz, at an interval of 5 s between each train. As this was a pilot study, each only received 1000 pulses in a single session.
Intervention Type
Device
Intervention Name(s)
Magnetic Stimulation with tilted coil
Intervention Description
The placebo arm consisted of 'sham' SMS delivered with the coil angled vertically and one of the wing edges in contact with the stimulation point. As this coil type allows maximum magnetic flux at the center of the intersection, we believe minimum or no stimulation was effected at the edge of the coil in contact with the patient. Stimulation parameters and duration were unchanged in this arm.
Primary Outcome Measure Information:
Title
Subjective pain score measurements
Description
NAS score
Time Frame
4 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All with neuropathic lower limb pain Exclusion Criteria: Contraindications to magnetic stimulation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
YL Lo, MD
Organizational Affiliation
National Neuroscience Institute, Singapore General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Singapore General Hospital
City
Singapore
ZIP/Postal Code
169608
Country
Singapore

12. IPD Sharing Statement

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Spinal Magnetic Stimulation in Neuropathic Pain

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