Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06467708

Transcutaneous Auricular Neurostimulation for ICU Patients With Traumatic Brain Injury

Led by University of Texas Southwestern Medical Center · Updated on 2026-02-18

42

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The overarching goal of this pilot study is to assess the feasibility and safety of transcutaneous auricular neurostimulation (tan) in ICU patients with TBi and to determine the effect of tan on serum markers of inflammation. exploratory analyses will examine effects on such physiological parameters as blood pressure, heart rate, and intracranial pressure (iCP), as well as measures of neurological function.

CONDITIONS

Official Title

Transcutaneous Auricular Neurostimulation for ICU Patients With Traumatic Brain Injury

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Post-resuscitation Glasgow Coma Scale score of 12 or below and acute trauma-related intradural blood on head CT scan after traumatic brain injury
  • Age 18 years or older
  • Consent obtained from the legally authorized representative
Not Eligible

You will not qualify if you...

  • Hemodynamic instability
  • Expected imminent death due to severe neurological or systemic injury
  • Unclear neurological status caused by paralytic medications or intoxication
  • Presence of implanted electrical stimulation devices such as pacemakers or cochlear prostheses
  • Abnormal ear anatomy or ear infection
  • Pregnancy or lactation
  • Significant medical or psychosocial issues that could harm the participant, affect participation, or influence trial results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

UT Southwestern Medical Center

Dallas, Texas, United States, 75390

Actively Recruiting

Loading map...

Research Team

A

Alex Valadka, MD

CONTACT

A

Aisha Qureshi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here