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NCT06016686RecruitingPhase 1

Microelectrode Recordings From the Vagus Nerve in Awake Humans

Source: ClinicalTrials.gov · Last updated 20 Apr 2026

Brief summary (registry, in English)

This Anchillary project uses a refined technique of ultrasound-guided microneurography of the human cervical vagus nerve, an approach developed by Professor Vaughan Macefield and used safely to-date in 44 prior study participants. The overall goal of this project is to build upon prior data obtained using this approach by undertaking a detailed neurophysiological investigation of the human vagus nerve and to identify the nerve fibers activated during vagal nerve stimulation (VNS) in participants with implanted VNS devices in response to different stimulation parameters. In addition to providing data in unprecedented detail into the physiology of the human vagus nerve, this project will investigate different stimulus intensities, durations and frequencies that differentially excite myelinated and unmyelinated nerve fibers. These results will inform the CSP and guide future development of novel neural interfaces for VNS for various clinical applications.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
60 (estimated)
First submitted
10 Jul 2023
Start date
1 Apr 2024
Primary completion date
31 Dec 2026
Lead sponsor
University of Minnesota
Diseases
Epilepsy
NCT number
NCT06016686

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 60
  • From 1 Apr 2024 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Pregnant
  • Smokes and is unwilling to abstain from smoking on the day of the experiment.
  • Inability or unwillingness to provide written informed consent.
  • Individuals with difficulty standing unassisted for 5 minutes during the tilt-table testing
  • Individuals found to have a significant carotid artery plaque or intima-media thickness \> 1 mm as assessed by ultrasonography during the ultrasound-screening steps of the study visit
  • Vagus nerve not visible on ultrasound
  • VNS electrodes are not in a suitable location to allow for microelectrode insertion
  • Any other clinical reasons deemed by the investigators

Who the study is looking for

  • The participant is greater than or equal to (≥)18 years and is less than or equal to (≤) 40 years of age
  • English speaking
  • Medicare covered or equivalent health insurance from a partner country

Age in the registry: 18 years to 40 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Minnesota
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.