RM1 Project 1 - tAN Naloxone

Recruiting Early Phase 1 Interventional Study
Analgesia
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Early Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
136 (estimated)
Sponsor
Medical University of South Carolina · Other
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About This Trial
This two-visit, randomized, double-blind, sham-controlled trial, uses a novel naloxone blockade model in 136 individuals to determine whether the analgesic effects of a 30-minute transcutaneous auricular neurostimulation (tAN) intervention are mediated through a release of endogenous opioids. Analgesic effects of four various stimulation interventions will be measured (auricular vagus, auricular t…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age 18-65 * Have the capacity and ability to provide one's own consent and sign the informed consent document Exclusion Criteria: * Contraindicated for MRI. * Any current or recent untreated medical, neurological, or psychiatric conditions * Metal implant devices in the head…
Contacts

Bashar Badran, PhD

8437926076

badran@musc.edu

CONTACT