MC5-A Scrambler Therapy for the Treatment of Chronic Neuropathic Extremity Pain

Status unconfirmed · Not applicable · Has a placebo group

Conditions studied: Peripheral Neuropathy, Low Back Pain

In brief

The FDA-approved MC5-A Scrambler Therapy (MC5-A ST) is an electroanalgesia device that interferes with pain signal transmission by using nerve fibers as a passive means to convey a message of normality (sans pain) to the central nervous system. While preliminary research has demonstrated its efficacy in treating chronic neuropathic pain secondary to cancer and failed back surgery syndrome, its effectiveness in treating chronic neuropathic pain secondary to traumatic musculoskeletal injuries like those experienced in combat has not been investigated. The purpose of this prospective, double-blind, randomized controlled, study is to determine if the MC5-A ST is efficacious in altering the biological, psychological, and social components of the chronic neuropathic pain experience in military Service Members (SMs) with traumatic musculoskeletal extremity injuries.

Key facts

Study ID

NCT02701075

Run by

Brooke Army Medical Center

People needed

58

Starts

2013-09-01

Expected to finish

2017-08-31

Last updated by the study team

2017-02-07

Who can join

Age: 18 and older, up to 79. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• military service members (active duty \& retirees) between the ages of 18 and 79, inclusive
• neuropathic pain symptoms present for 3 months or greater prior to entry into the study
• rated pain intensity equal to or greater than 3 on NRS-11 pain scale
• painful peripheral neuropathy in an extremity that is the result of a traumatic injury (post-traumatic/ post-surgical neuropathy, stump pain, entrapment neuropathy), or low back pain with radiculopathy
• stable pain medication treatment regimen
• able to speak and read English, understand the study procedures, and consent to study participation

You may not qualify if…

• pacemaker or other implantable devices
• vena cava, aneurysm clips, coronary or other vascular stents
• pregnancy via a pregnancy test
• history of epilepsy, brain injury, symptomatic brain metastases
• prior celiac plexus block, or other neurolytic pain control treatment, within 4 weeks
• wounds or skin irritation in areas where the electrodes are required to be placed
• cardiac ischemia within the previous 6 months
• severe arrhythmia
• documented history of moderate or severe traumatic brain injury
• latex allergies
• open wound over site of chronic pain
• unable to stop anti-epileptic medications or gabapentin over 2 weeks of MC5-A ST treatment
• history of electroanalgesia treatment (electroacupuncture, biomodulator, TENS) over last 30 days
• participation in the study would delay the medical board (MEB) processing of the service member off of active duty status or would delay a return to duty status to their home unit.
• metal implants such as cardiac pacemakers, automatic defibrillators, aneurysm clips, vena cava clips and skull plates

Where it is running

• Brooke Army Medical Center — Fort Sam Houston, Texas, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.