Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
96 participants
INTERVENTIONAL
2023-03-17
2027-10-01
Brief Summary
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Detailed Description
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Stimulation of the ABVN has demonstrated additional benefits for reducing the need for opioids for pain as well as lessening opioid withdrawal symptoms. Clinical trials of ABVN stimulation as an adjunctive treatment for pain have noted decreased intake of tramadol , remifentanil, morphine, as well as naproxen plus tramadol. A pioneering study of electrical stimulation at the cymba conchae in eight persons with opioid use disorder found significantly reduced withdrawal symptoms: first, decreases in anxiety, craving for opioids, chills, nausea; second, reduced bone and joint pain. Results in follow-up clinical trials bolstered the efficacy of ABVN stimulation for opioid withdrawal . More recently, an open-label trial of simultaneous ABVN and trigeminal stimulation found reduced withdrawal symptoms and decreased need for morphine maintenance in newborns with neonatal opioid withdrawal syndrome . This method of simultaneous vagal and trigeminal stimulation via the external ear is known as transcutaneous auricular neurostimulation (tAN), as the targets of electrical stimulation include the ABVN and auriculotemporal nerve (ATN), which is a branch of the mandibular division of the trigeminal nerve. Electrodes applied to select dermatome regions can target ear neural structures and deliver non-invasive vagus nerve stimulation (VNS) and trigeminal nerve stimulation (TNS). See Figure 1.
Use of tAN devices for pain relief is an attractive alternative to pharmacologic and opioid-based approaches because it is safe and effective and presents no addiction liability. In order to increase clinical adoption and optimize efficacy of these devices, the mechanism of action must be fully characterized.
This study is investigating the mechanism behind tAN in a healthy cohort. Using tAN combined with advanced neuroimaging, we hope to begin to understand what parts of the brain are activated during tAN, compared to sham.
Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
TREATMENT
DOUBLE
Study Groups
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Auricular Neurostimulation (Active 1)
•Within the MRI scanner, each participant will be connected to a series of tAN electrodes that stimulate the following ear target
-ABVN Only stimulation (15Hz stimulation of cymba conchae)
Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Auricular Neurostimulation (Active 2)
•Within the MRI scanner, each participant will be connected to a series of tAN electrodes that stimulate the following ear target
-ATNS Only stimulation (100Hz stimulation of the tragus)
Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Auricular Neurostimulation (Active 3)
•Within the MRI scanner, each participant will be connected to a series of tAN electrodes that stimulate the following ear target
-Combo stimulation (stimulation of both the 15Hz cymba conchae and 100HZ tragus)
Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Auricular Neurostimulation (Sham 1)
•Within the MRI scanner, each participant will be connected to a series of tAN electrodes that stimulate the following ear target
-Sham (15Hz stimulation of the earlobe)
Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Auricular Neurostimulation (Sham 2)
•Within the MRI scanner, each participant will be connected to a series of tAN electrodes that stimulate the following ear target
-Sham (100Hz stimulation of the earlobe)
Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Interventions
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Transcutaneous Auricular Neruostimulation (tAN)
The intervention we are studying is called transcutaneous auricular neurostimulation (tAN). tAN is simply electrical nerve stimulation administered at the ear which targets both the auricular branch of the vagus nerve (ABVN) and the auriculotemporal nerve (ATN, a branch of the trigeminal nerve).
Eligibility Criteria
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Inclusion Criteria
* Have the capacity and ability to provide one's own consent and sign the informed consent document
Exclusion Criteria
* Any current or recent untreated medical, neurological, or psychiatric conditions
* Metal implant devices in the head, heart or neck.
* History of brain surgery.
* History of myocardial infarction or arrhythmia, bradycardia.
* Personal or family history of seizure or epilepsy or personal use of medications that substantially reduce seizure threshold (e.g., olanzapine, chlorpromazine, lithium).
* Personal history of head injury, concussion, or self-report of moderate to severe traumatic brain injury.
* Individuals suffering from frequent/severe headaches.
* Individuals with a reported history of psychosis or mania, or individuals who are actively manic or psychotic.
* Moderate to severe alcohol or substance use disorder.
* Pregnancy
18 Years
65 Years
ALL
Yes
Sponsors
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Medical University of South Carolina
OTHER
Responsible Party
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Jeffrey Borckardt
Assistant Professor
Locations
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Medical University of South Carolina Institute of Psychiatry
Charleston, South Carolina, United States
Countries
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Central Contacts
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Facility Contacts
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Bashar W Badran, PhD
Role: primary
Other Identifiers
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Pro00122682
Identifier Type: -
Identifier Source: org_study_id