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RECRUITING NA

Transcutaneous Auricular Vagus Enhanced Recovery in the NeuroICU

NCT07219108 · View on ClinicalTrials.gov ↗

Study Summary

This study will demonstrate the impact of taVNS on reducing adverse events in NeuroICU patients, determine if taVNS reduces length of stay, and quantify the economic benefits of taVNS implementation in a broader neurocritical care population.

Interventions

  • DEVICE Auricular Vagus Nerve Stimulation
  • DEVICE Sham Auricular Vagus nerve Stimulation

Study Locations (1)

Missouri

  • Washington University School of Medicine — St Louis

Trial Details

FieldValue
Enrollment Target 160 participants
Start Date 2025-09-24
Est. Completion 2027-09-23
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07219108

The ClinicalTrials.gov registry entry for NCT07219108 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 160 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,036 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Acute Medical Conditions appearing as the primary indexed condition, and to 2 interventions — of which Auricular Vagus Nerve Stimulation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07219108 reports 1 study location spanning 1 distinct geographic area — top geographies include Missouri. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07219108 about?

NCT07219108 is a clinical study titled "Transcutaneous Auricular Vagus Enhanced Recovery in the NeuroICU". This study will demonstrate the impact of taVNS on reducing adverse events in NeuroICU patients, determine if taVNS reduces length of stay, and quantify the economic benefits of taVNS implementation in a broader neurocritical care population.

What is the current status of trial NCT07219108?

This trial is currently recruiting. It is a NA study. The enrollment target is 160 participants. The study started on 2025-09-24. Estimated completion is 2027-09-23.

What conditions does trial NCT07219108 study?

This clinical trial studies the following conditions: Acute Medical Conditions, Acute Neurological Injury. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07219108?

The interventions under investigation include: Auricular Vagus Nerve Stimulation (DEVICE), Sham Auricular Vagus nerve Stimulation (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07219108?

This trial is sponsored by Washington University School of Medicine, which has 1,036 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07219108 being conducted?

This trial has 1 study location across Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial