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Effectiveness of Acupuncture in Relieving Pain Due to Fibromyalgia

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Acupuncture
Sham treatment
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring acupuncture, analgesia, pain, fibromyalgia, fMRI, PET

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: fMRI Inclusion Criteria: Has met American College of Rheumatology (1990) criteria for the diagnosis of fibromyalgia for at least 1 year Chronic pain more than 50% of days Willing to limit introduction of any new medications or treatments for fibromyalgia during the study Able to attend study visits up to three times weekly Right-handed Must be within driving distance of Ann Arbor, MI PET Inclusion Criteria: Meets fMRI inclusion criteria Willing to refrain from alcohol intake for 48 hours prior to PET studies Exclusion Criteria: fMRI Exclusion Criteria: Knowledge that could prevent "blinding" of the participant to the study interventions (including previous acupuncture treatment) Presence of a known coagulation abnormality, thrombocytopenia, or bleeding diathesis that may preclude the safe use of acupuncture Autoimmune or inflammatory disease (in addition to fibromyalgia) that causes pain (e.g., rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease) Daily use of narcotic pain-relievers History of substance abuse Simultaneous participation in other therapeutic trials Pregnant or breastfeeding Current severe psychiatric illness (e.g., schizophrenia, major depression with suicidal ideation) Condition that may make exposure to fMRI medically inadvisable Any condition that may prevent satisfactory completion of the study protocol PET Exclusion Criteria: Meets any of the fMRI exclusion criteria Current major depression Condition that may make exposure to PET medically inadvisable

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Traditional Acupuncture

Sham Treatment

Arm Description

Acupuncture sites will be used for active intervention.

Sham acupuncture is used.

Outcomes

Primary Outcome Measures

Change in Mu-opioid Receptor Occupancy
Here we report the change (post - pre) in mu-opioid receptor binding potential (BP) for the perigenual anterior cingulate. BP is a unitless measure and reflects the total maximum binding of receptors divided by the dissociation constant. BP = Bmax/Kd.

Secondary Outcome Measures

Full Information

First Posted
September 1, 2005
Last Updated
April 9, 2015
Sponsor
University of Michigan
Collaborators
National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT00142597
Brief Title
Effectiveness of Acupuncture in Relieving Pain Due to Fibromyalgia
Official Title
Mechanisms of Acupuncture Analgesia
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
May 2005 (undefined)
Primary Completion Date
March 2011 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

5. Study Description

Brief Summary
This study will determine the effectiveness of acupuncture versus a placebo in altering brain activity and relieving pain due to fibromyalgia.
Detailed Description
Fibromyalgia is one of the most common rheumatic diseases, second only to osteoarthritis. It causes chronic muscle pain and fatigue. Acupuncture functions by targeting specific nerve pathways to different organs or parts of the body. Research has shown that acupuncture is effective in decreasing or eliminating people's sensitivity to pain in targeted regions. However, some believe that the reduction in pain is due to a placebo response rather than acupuncture itself. This study will use two brain-imaging techniques to determine the brain response to acupuncture versus a simulation of acupuncture, thereby assessing whether acupuncture is actually effective in relieving pain. Participants in this single-blind study will be randomly assigned to receive either acupuncture or a placebo treatment. The placebo will consist of a simulation of acupuncture. Functional magnetic resonance imaging (fMRI) and positron emission tomography (PET) will be used to assess activity of brain mu-opioid receptors. These receptors are involved in the body's ability to perceive pain. All participants will be scanned twice using the fMRI scanner, once before any treatment sessions and once at the conclusion of all treatment sessions. Both fMRI sessions will involve applying pressure to the thumb to elicit a response in the brain in order to assess the corresponding fMRI blood oxygen level dependent (BOLD) signal and whether this activation changes after treatment intervention. Participants will then receive nine treatments of acupuncture or placebo outside the scanner over a 4-week period. The PET portion of this study is optional, and, if you elect to participate, your first treatment session will be performed in the PET scanner. After this first session, participants will have seven additional treatment sessions outside of the scanner over a 4-week period. The last session will be performed in the PET scanner to assess changes in mu-opioid receptor activity that may have occurred over the 4 weeks. A baseline visit to determine eligibility and a close-out visit at week 8 are also part of the participation schedule. It is very important that participants live within driving distance of Ann Arbor, MI due to the significant number of visits to our Center.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
acupuncture, analgesia, pain, fibromyalgia, fMRI, PET

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
46 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Traditional Acupuncture
Arm Type
Active Comparator
Arm Description
Acupuncture sites will be used for active intervention.
Arm Title
Sham Treatment
Arm Type
Sham Comparator
Arm Description
Sham acupuncture is used.
Intervention Type
Device
Intervention Name(s)
Acupuncture
Intervention Description
Involves the insertion and manual stimulation of thin acupuncture needles into specific points in the body. Fibromyalgia participants will be randomized to receive 9 acupuncture treatments over the course of four weeks. All participants will be scanned twice using the fMRI scanner. The PET portion of the study is optional.
Intervention Type
Other
Intervention Name(s)
Sham treatment
Intervention Description
Fibromyalgia participants will be randomized to receive 9 sham treatments over the course of four weeks. All participants will be scanned twice using the fMRI scanner. The PET portion of the study is optional.
Primary Outcome Measure Information:
Title
Change in Mu-opioid Receptor Occupancy
Description
Here we report the change (post - pre) in mu-opioid receptor binding potential (BP) for the perigenual anterior cingulate. BP is a unitless measure and reflects the total maximum binding of receptors divided by the dissociation constant. BP = Bmax/Kd.
Time Frame
measured from baseline to week 5

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: fMRI Inclusion Criteria: Has met American College of Rheumatology (1990) criteria for the diagnosis of fibromyalgia for at least 1 year Chronic pain more than 50% of days Willing to limit introduction of any new medications or treatments for fibromyalgia during the study Able to attend study visits up to three times weekly Right-handed Must be within driving distance of Ann Arbor, MI PET Inclusion Criteria: Meets fMRI inclusion criteria Willing to refrain from alcohol intake for 48 hours prior to PET studies Exclusion Criteria: fMRI Exclusion Criteria: Knowledge that could prevent "blinding" of the participant to the study interventions (including previous acupuncture treatment) Presence of a known coagulation abnormality, thrombocytopenia, or bleeding diathesis that may preclude the safe use of acupuncture Autoimmune or inflammatory disease (in addition to fibromyalgia) that causes pain (e.g., rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease) Daily use of narcotic pain-relievers History of substance abuse Simultaneous participation in other therapeutic trials Pregnant or breastfeeding Current severe psychiatric illness (e.g., schizophrenia, major depression with suicidal ideation) Condition that may make exposure to fMRI medically inadvisable Any condition that may prevent satisfactory completion of the study protocol PET Exclusion Criteria: Meets any of the fMRI exclusion criteria Current major depression Condition that may make exposure to PET medically inadvisable
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard E. Harris, PhD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18311814
Citation
Harris RE, Sundgren PC, Pang Y, Hsu M, Petrou M, Kim SH, McLean SA, Gracely RH, Clauw DJ. Dynamic levels of glutamate within the insula are associated with improvements in multiple pain domains in fibromyalgia. Arthritis Rheum. 2008 Mar;58(3):903-7. doi: 10.1002/art.23223.
Results Reference
derived

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Effectiveness of Acupuncture in Relieving Pain Due to Fibromyalgia

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