Prospective Evaluation of RINCE to Reduce Fibromyalgia Effects - 301

NCT ID: NCT02211508

Last Updated: 2016-08-09

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 236 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-07-31
• Study Completion Date: 2015-02-28

Brief Summary

The purpose of this study is to test the safety and efficacy of a noninvasive cortical electrostimulation therapy known as "Reduced Impedance Noninvasive Cortical Electrostimulation" (RINCE) in the treatment of pain associated with fibromyalgia. Patients who meet the 2010 American College of Rheumatology criteria for fibromyalgia will receive up to 24 RINCE treatments delivered by a medical device called "NeuroPoint". Approximately 200 fibromyalgia patients will be randomized into one of two study groups. One of these groups will receive sham treatment, meaning they will receive no treatment at all, while the other group will receive active RINCE treatment. The study's primary outcome measure will be the difference between active and sham treatment groups in the mean change from baseline in patients' weekly worst pain scores. The study's hypothesis is that there will be a difference between treatment groups in primary outcome measure.

Conditions

Fibromyalgia

Study Design

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

Study Groups

12-week RINCE

RINCE - active RINCE therapy involving 24 total treatment applications from NeuroPoint device

Group Type: ACTIVE_COMPARATOR

RINCE

Intervention Type: DEVICE

The NeuroPoint device is used to deliver repeat applications of RINCE therapy

Sham RINCE

Sham RINCE - sham RINCE therapy involving 24 total sham applications from NeuroPoint device

Group Type: SHAM_COMPARATOR

RINCE

Intervention Type: DEVICE

The NeuroPoint device is used to deliver repeat applications of RINCE therapy

Interventions

RINCE

The NeuroPoint device is used to deliver repeat applications of RINCE therapy

Intervention Type: DEVICE

Other Intervention Names

RINCE therapy; RINCE therapy delivered by the NeuroPoint device

Eligibility Criteria

Inclusion Criteria

• Patient is male or female, 22 to 65 years of age, inclusive.
• Patient has a diagnosis of primary fibromyalgia as defined by the 2010 American College of Rheumatology Preliminary Diagnostic Criteria for fibromyalgia.
• If female, is either not of childbearing potential or is willing to utilize specified practices throughout the study to prevent becoming pregnant.
• Patient is willing and able to refrain or withdraw from the following therapies for the duration of the study: duloxetine, milnacipran, pregabalin, gabapentin, naltrexone, sodium oxybate, and opiates.
• Qualified patients with mild or moderate depression must be clinically stable, without risk of suicidal ideation or behavior, and the dose of allowed anti-depressants should have been stable for at least three months prior to the Baseline clinic visit.
• Patient is willing and able to comply with all protocol-specified requirements.
• Patient is capable of reading and understanding English and has provided written informed consent to participate.

Exclusion Criteria

• The patient suffers from one or more of clinically significant psychiatric condition that could interfere with the patient's well-being or ability to comply with the protocol.
• Patient has a Beck Depression Inventory-II total score greater than 25 at either the Screening visit or Baseline clinic visit.
• The patient is at increased risk of suicide.
• Patient is unable, unwilling or not advised to refrain from or discontinue prohibited medications or treatments.
• Patient has a diagnosis of, or is being treated for, systemic lupus erythematosus, inflammatory arthritis, or other documented systemic autoimmune disorder, Parkinson's disease, multiple sclerosis, or cancer (other than basal or squamous cell skin cancer).
• Patient has any other chronic pain condition that, in the Investigator's or Sponsor's opinion, could interfere with the patient's assessment of his/her fibromyalgia status.
• Patient has a history of severe, refractory or uncontrolled migraine headaches, seizure disorder or clinically significant cognitive dysfunction.
• Patient is pregnant or planning to become pregnant within the next 6 months.
• Patient has a body mass index greater than 40 at the Screening visit.
• Patient has a history of cranial electrical stimulation or transcutaneous magnetic stimulation within 2 years of screening, or electroconvulsive therapy within 5 years of screening.
• Patient has a metal implant at or above the level of the 7th cervical vertebra, a cardiac pacemaker or defibrillator, or vagus nerve stimulator.
• Any recent surgery or anticipated need for surgery that might confound results or interfere with patient's ability to comply with the protocol.
• Myocardial infarction during the 12 months prior to screening, uncontrolled hypertension, active cardiac disease, clinically significant cardiac rhythm or conduction abnormality, or anticipation of bypass or other cardiac surgery within the next 12 months.
• Current systemic infection (e.g., HIV, hepatitis B or C; Lyme disease).
• Patient is using opiates on a regular or frequent basis.
• Pending or current litigation or disability claim (including Workman's Compensation).
• History of significant alcohol and/or drug abuse or dependency within preceding 5 years, or a positive result on the screening (or subsequent) drug screen indicating use of an illicit substance.
• Patient has participated in an investigational study of a therapeutic treatment within 90 days prior to Screening visit or is currently participating in another clinical trial.

• Minimum Eligible Age: 22 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cerephex Corporation

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

R. Michael Gendreau, MD PhD

Role: STUDY_DIRECTOR

Cerephex Corporation

Locations

Achieve Clinical Research, LLC

Birmingham, Alabama, United States

Premier Research

Phoenix, Arizona, United States

Neurovations

Napa, California, United States

Superior Research LLC

Sacramento, California, United States

Artemis Institute for Clinical Research

San Diego, California, United States

Avail Clinical Research

DeLand, Florida, United States

Compass Research LLC

Orlando, Florida, United States

Chicago Research Center

Chicago, Illinois, United States

Michigan Head Pain & Neurological Institute

Ann Arbor, Michigan, United States

Fieve Clinical Research

New York, New York, United States

Upstate Clinical Research Associates

Williamsville, New York, United States

University of Cincinnati College of Medicine

Cincinnati, Ohio, United States

Sunstone Medical Research

Medford, Oregon, United States

Omega Medical Research

Warwick, Rhode Island, United States

Fatigue Consultation Clinic

Salt Lake City, Utah, United States

Swedish Clinical Research

Seattle, Washington, United States

Countries

United States

References

Hargrove JB, Bennett RM, Simons DG, Smith SJ, Nagpal S, Deering DE. A randomized placebo-controlled study of noninvasive cortical electrostimulation in the treatment of fibromyalgia patients. Pain Med. 2012 Jan;13(1):115-24. doi: 10.1111/j.1526-4637.2011.01292.x.

Reference Type: BACKGROUND

PMID: 22233397 (View on PubMed)

Hargrove JB, Bennett RM, Clauw DJ. Long-term outcomes in fibromyalgia patients treated with noninvasive cortical electrostimulation. Arch Phys Med Rehabil. 2012 Oct;93(10):1868-71. doi: 10.1016/j.apmr.2012.04.006. Epub 2012 Apr 21.

Reference Type: BACKGROUND

PMID: 22525670 (View on PubMed)

Other Identifiers

NPT-301

Identifier Type: -

Identifier Source: org_study_id