Evaluation of Magnetic Fields to Treat Fibromyalgia

NCT ID: NCT01262131

Last Updated: 2011-07-01

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 13 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-12-31
• Study Completion Date: 2011-05-31

Brief Summary

The purpose of this study is to see if a device called the Resonator can help to reduce pain and improve aspects of health and quality of life for people with fibromyalgia.

Detailed Description

The purpose of this pilot study is to assess the efficacy of the Resonator device as an adjunctive therapy to reducing pain and improving aspects of health and quality of life that are relevant to individuals with fibromyalgia.

Conditions

Fibromyalgia

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Resonator Protocol A

Group Type: ACTIVE_COMPARATOR

magnetic therapy protocol A

Intervention Type: DEVICE

Application of magnetic fields using the Resonator device Protocol A

Resonator Protocol B

Application of magnetic fields using the Resonator device Protocol B

Group Type: ACTIVE_COMPARATOR

magnetic therapy Protocol B

Intervention Type: DEVICE

Application of magnetic fields using the Resonator device Protocol B

Inactive Resonator

Group Type: PLACEBO_COMPARATOR

placebo therapy

Intervention Type: DEVICE

Application of inactive magnetic fields using the Resonator device

Interventions

magnetic therapy protocol A

Application of magnetic fields using the Resonator device Protocol A

Intervention Type: DEVICE

magnetic therapy Protocol B

Application of magnetic fields using the Resonator device Protocol B

Intervention Type: DEVICE

placebo therapy

Application of inactive magnetic fields using the Resonator device

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• Current diagnosis of fibromyalgia made by the study Principal Investigator (PI) according to the American College of Rheumatology 1990 Criteria for the Classification of Fibromyalgia.
• Rating of current Degree of Pain on the 0-10 Numeric Pain Intensity Scale of 4 or greater.
• Subject's use of pain relief medication(s) has been stable over the past 30 days, and subject is willing and able to maintain pre-existing use of pain relief medication(s) as his or her sole pain relief medication use, as needed, throughout study participation.
• Subject's use of insomnia medication(s) has been stable over the past 30 days, and subject is willing and able to maintain this existing use of insomnia medication(s) as his or her sole insomnia relief medication(s), as needed, throughout study participation.
• Subject has been on current (or no) medication regimen, unchanged for at least 30 days prior to study enrollment, and is willing and able to maintain that regular medication regimen, unchanged, throughout study participation.
• Willing and able to refrain from use of tender point injections throughout study participation.
• Willing and able to abstain from partaking in other/new treatments to improve fibromyalgia symptoms during study participation.
• Adequate contraceptive measures for female subjects. > 18 years of age or older.
• Male or female.

Exclusion Criteria

• Any factors that might prevent the subject from completing a full course of therapy with the Resonator™ device, or from attending any of the scheduled study visits, or from completing any of the study measures.
• Subject suffers from co-existent chronic pain condition(s) of non-fibromyalgia origin, such as osteoarthritis, low back pain, neck pain, painful diabetic neuropathy and postherpetic neuropathic pain, that cannot be distinguished in severity and/or in type/sensation of pain from the pain originating from the subject's condition of fibromyalgia.
• Any other significant comorbidities that might impact the ability to evaluate the subject's satisfaction of the ACR 1990 Criteria for the Classification of Fibromyalgia, or for the subject to complete any of the study assessment tools.
• Tender point injections received within the prior one month.
• Current or past history of major psychiatric disturbance (e.g., schizophrenia, bipolar disorder, substance abuse).
• Known inflammatory rheumatic disease.
• Epilepsy/history of seizures/taking medication for epilepsy.
• HIV and other autoimmune disorders.
• Active cancer or treatment for cancer within last 6 months.
• Active infection(s).
• History of ECT
• Uncontrolled Hypertension.
• Advanced Pulmonary Disease.
• Unstable cardiac disease.
• Prosthetics or implants comprised of ferrous metals.
• Pacemakers, vagus nerve stimulators, or other functional electrical stimulators such as those commonly used for pain.
• Consumption of more than 21 alcoholic drinks per week.
• Pregnant, breast feeding, or planning pregnancy prior to end of study participation.
• Developmental disability or other cognitive impairment that would in the judgment of the PI impair adequate comprehension of the informed consent form or complete any of the study-related activities.
• Worker's compensation, receipt of disability or present/past litigation for monetary compensation pertaining to subject's fibromyalgia condition.
• Participation in other research within 30 days of study enrollment.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

pico-tesla Magnetic Therapies, LLC

INDUSTRY

Sponsor Role: lead

Responsible Party

Pico-Tesla Magnetic Therapies, LLC

Principal Investigators

Jerry I Jacobson, Ph.D, D.M.D.

Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

10242-01

Identifier Type: -

Identifier Source: org_study_id