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Influence of Transcranial Direct Current Stimulation of the Primary Motor Cortex on Pain Sensation in Patients Suffering From Fibromyalgia Syndrome

Primary Purpose

Fibromyalgia

Status
Terminated
Phase
Phase 4
Locations
Austria
Study Type
Interventional
Intervention
transcranial direct current stimulation
sham treatment
Sponsored by
Karl Landsteiner Institute of Remobilization and Functional Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring widespread chronic pain, transcranial direct current stimulation, fibromyalgia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All Sexes

Inclusion Criteria:

  • Patients who have an established diagnosis of fibromyalgia according to the 1990 criteria of the "American College of Rheumatology"
  • Symptoms have been present at a similar level for at least 3 months
  • Stable medication for at least 2 months
  • visual analog scale ≥ 3 (0=no pain; 10=worst possible pain)
  • The patient does not have a disorder that would otherwise explain the pain

Exclusion Criteria:

  • Alcohol/substance abuse
  • Pregnancy
  • Neuropsychiatric disorders
  • Metal implants near stimulation area
  • Cardiac pace maker
  • Local injuries
  • Inflammatory rheumatic disease
  • Acute tumor
  • Acute fracture
  • Well-defined neuropathic induced pain

Sites / Locations

  • Karl Landsteiner Institute of Remobilisation and Functional Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

transcranial direct current stimulation

sham treatment

Arm Description

transcranial direct current stimulation of the primary motor cortex

Outcomes

Primary Outcome Measures

Visual Analoge Scale

Secondary Outcome Measures

Quality of Life - SF-36
Fibromyalgia Impact Questionaire
IL-10 ELISA
Visual analog scale
IL-6 ELISA
IL-4 ELISA
TNF-alpha ELISA

Full Information

First Posted
December 14, 2010
Last Updated
July 2, 2014
Sponsor
Karl Landsteiner Institute of Remobilization and Functional Health
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1. Study Identification

Unique Protocol Identification Number
NCT01261650
Brief Title
Influence of Transcranial Direct Current Stimulation of the Primary Motor Cortex on Pain Sensation in Patients Suffering From Fibromyalgia Syndrome
Official Title
Influence of Transcranial Direct Current Stimulation of the Primary Motor Cortex on Pain Sensation in Patients Suffering From Fibromyalgia Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Terminated
Why Stopped
There could not be enough patients recruited
Study Start Date
December 2010 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Karl Landsteiner Institute of Remobilization and Functional Health

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Fibromyalgia is a common chronic pain syndrome characterized by bad treatable chronic widespread pain present at a similar level for at least 3 months. The aim of this study is to examine if 3 weeks of transcranial direct current stimulation is a suitable therapy to reduce chronic pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
widespread chronic pain, transcranial direct current stimulation, fibromyalgia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
transcranial direct current stimulation
Arm Type
Active Comparator
Arm Description
transcranial direct current stimulation of the primary motor cortex
Arm Title
sham treatment
Arm Type
Sham Comparator
Intervention Type
Device
Intervention Name(s)
transcranial direct current stimulation
Intervention Type
Device
Intervention Name(s)
sham treatment
Primary Outcome Measure Information:
Title
Visual Analoge Scale
Time Frame
Difference Baseline - after treatment
Secondary Outcome Measure Information:
Title
Quality of Life - SF-36
Time Frame
baseline / after treatment / 1 , 2, 3 months after treatment
Title
Fibromyalgia Impact Questionaire
Time Frame
baseline / after treatment / 1,2,3, months after treatment
Title
IL-10 ELISA
Time Frame
baseline / after treatment / 1,2,3, months after treatment
Title
Visual analog scale
Time Frame
1,2,3 months after treatment
Title
IL-6 ELISA
Time Frame
baseline / after treatment / 1,2,3, months after treatment
Title
IL-4 ELISA
Time Frame
baseline / after treatment / 1,2,3, months after treatment
Title
TNF-alpha ELISA
Time Frame
baseline / after treatment / 1,2,3, months after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Eligibility Criteria
Inclusion Criteria: Patients who have an established diagnosis of fibromyalgia according to the 1990 criteria of the "American College of Rheumatology" Symptoms have been present at a similar level for at least 3 months Stable medication for at least 2 months visual analog scale ≥ 3 (0=no pain; 10=worst possible pain) The patient does not have a disorder that would otherwise explain the pain Exclusion Criteria: Alcohol/substance abuse Pregnancy Neuropsychiatric disorders Metal implants near stimulation area Cardiac pace maker Local injuries Inflammatory rheumatic disease Acute tumor Acute fracture Well-defined neuropathic induced pain
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael Quittan, PhD
Organizational Affiliation
Karl Landsteiner Institute of Remobilisation and functional Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karl Landsteiner Institute of Remobilisation and Functional Health
City
Vienna
ZIP/Postal Code
1100
Country
Austria

12. IPD Sharing Statement

Learn more about this trial

Influence of Transcranial Direct Current Stimulation of the Primary Motor Cortex on Pain Sensation in Patients Suffering From Fibromyalgia Syndrome

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