Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT06381102 · ClinicalTrials.gov registry record · NA

Transcutaneous Vagus Nerve Stimulation (taVNS) Dosage Study 1

A NA study, sponsored by University of Miami.

Completed
Registry status
NA
Development phase
31
Enrollment target

NCT06381102: Completed NA study, sponsored by University of Miami.

NCT06381102 is a NA study that has completed, run by University of Miami. The registered enrollment target is 31 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06381102, a NA study, has completed, sponsored by University of Miami.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target

Study Summary

The purpose of this research study is to investigate the effects of different forms of a gentle form of electrical stimulation applied to the ear, known as transcutaneous auricular vagus nerve stimulation (taVNS). The research team is interested in how the different forms affect comfort and tolerability, as well as how well it works.

Primary Outcome

Tolerability will be assessed with a questionnaire with scores ranging from 0 -10 (with 0 being no irritation or discomfort and 10 being the worst possible irritation or discomfort) for irritation from tingling/tickling/pricking during taVNS.

Interventions

  • DEVICE transcutaneous auricular vagus nerve stimulation 30/30
  • DEVICE transcutaneous auricular vagus nerve stimulation 10/10

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2024-04-13
Est. Completion 2024-10-01
Phase NA
University of Miami

721 total trials

What the finished NCT06381102 record still lists

NCT06381102 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which transcutaneous auricular vagus nerve stimulation 30/30 is the first listed.

NCT06381102 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06381102 about?

NCT06381102 is a clinical study titled "Transcutaneous Vagus Nerve Stimulation (taVNS) Dosage Study 1". The purpose of this research study is to investigate the effects of different forms of a gentle form of electrical stimulation applied to the ear, known as transcutaneous auricular vagus nerve stimulation (taVNS). The research team is interested in how the different forms affect comfort and tolerabi...

What is the current status of trial NCT06381102?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2024-04-13. Estimated completion is 2024-10-01.

What interventions are being tested in trial NCT06381102?

The interventions under investigation include: transcutaneous auricular vagus nerve stimulation 30/30 (DEVICE), transcutaneous auricular vagus nerve stimulation 10/10 (DEVICE).

Who is sponsoring clinical trial NCT06381102?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06381102's enrollment target sits among peer trials

31 1592nd of 2000 higher than 408 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02932618 · 31 participants · Phase 3

    A Study of Recombinant Von Willebrand Factor (rVWF) With or Without ADVATE in Children With Severe Von Willebrand Disease (VWD)

  • NCT03482297 · 31 participants · Phase 1

    Automated Abdominal Binder for Orthostatic Hypotension

  • NCT04016389 · 31 participants · NA

    FIGO 2018 Stage IB2 Cervical Cancer Treated With Neoadjuvant Chemotherapy Followed by Fertility Sparing Surgery

  • NCT04211675 · 31 participants · Phase 1

    NK Cells Infusions With Irinotecan, Temozolomide, and Dinutuximab

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT06381102, the US trial registry maintained by the National Library of Medicine. NCT06381102 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.