Remote Electrical Neuromodulation for Migraine
What You Need to Know Before You Apply
What is the purpose of this trial?
Migraine and Fibromyalgia (FM) are chronic pain disorders characterized by altered central pain processing and impaired endogenous pain inhibition. FM presents with widespread musculoskeletal pain, fatigue, sleep disturbance, and cognitive symptoms and is strongly associated with central sensitization. Migraine similarly involves dysfunction of central inhibitory and descending pain modulation, with evidence of abnormal cortical excitability, impaired sensory habituation, and alterations in pain-related evoked potentials.
Conditioned Pain Modulation (CPM) is a measure of the body's endogenous pain-inhibitory mechanism, based on the phenomenon whereby the pain evoked by one painful stimulus (the test stimulus) is reduced by the concurrent application of a second, remote nociceptive stimulus (the conditioning stimulus). It is widely regarded as a proxy for the function of descending pain-modulatory pathways.
CPM is used as an experimental biomarker of descending pain inhibition across chronic pain conditions, including fibromyalgia and migraine. Studies consistently demonstrate reduced inhibitory responses in both migraine and fibromyalgia compared with healthy controls, indicating a robust deficit in descending pain modulatory systems. Combining a contact heat test stimulus (TS) with a cold pressor conditioning stimulus (CS) is a widely used and validated CPM paradigm.
Nerivio, a Remote Electrical Neuromodulation (REN) device, is a non-invasive, non-pharmacological therapy indicated for the acute and preventive treatment of migraine. The REN device is worn on the upper arm and delivers peripheral electrical stimulation to activate CPM-related descending inhibitory pathways and reduce migraine pain. This distal stimulation approach is designed to activate CPM-related circuits by recruiting brainstem pain-regulatory centers and modulating central nociceptive processing.
This randomized, double-blind, placebo-controlled trial is designed to assess the effect of a single REN session on CPM and cortical pain processing in adults with migraine or fibromyalgia. Using a standardized CPM induction protocol, the study will evaluate changes in behavioral CPM responses, before, during, and after REN vs. sham stimulation in patients with migraine or fibromyalgia. This study aims to clarify whether REN enhances descending pain inhibition and pain processing in populations with impaired endogenous pain modulation.
Who Is on the Research Team?
Alit Stark Inbar, PhD
Principal Investigator
Theranica
Are You a Good Fit for This Trial?
This trial is for adults diagnosed with migraine or fibromyalgia. Participants should not have other major health issues that could interfere with the study, and must be able to use a wearable device on their upper arm.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Remote Electrical Neuromodulation (REN) device
Trial Overview
The study tests a wearable device called Remote Electrical Neuromodulation (REN), which delivers mild electrical stimulation to the upper arm, against a placebo device. It aims to see if REN can improve how the body naturally reduces pain in people with migraine or fibromyalgia.
How Is the Trial Designed?
2
Treatment groups
Active Control
Placebo Group
This arm will use the active REN device as the Conditioned Stimulus (CS) to the thermal Test Stimulus (TS) that will be applied at 20, 40, and 60 minutes following the initiation of the treatment with the Active REN device.
This arm will use the Placebo device as the Conditioned Stimulus (CS) to the thermal Test Stimulus (TS) that will be applied at 20, 40, and 60 minutes following the initiation of the treatment with the Placebo device.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Theranica
Lead Sponsor
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