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NCT06543277 · ClinicalTrials.gov registry record · NA

Safety and Feasibility of Paired Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) With Upper Limb Rehabilitation in Incomplete Spinal Cord Injury

A NA study of Chronic Incomplete Cervical Spinal Cord Injury (SCI), sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
12
Enrollment target
2
Study locations

NCT06543277 is a NA study of Chronic Incomplete Cervical Spinal Cord Injury (SCI) that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 12 participants. The trial reports 2 study locations across 1 state.

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The verdict

NCT06543277, a NA study of Chronic Incomplete Cervical Spinal Cord Injury (SCI), is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
12 participants
Enrollment target
2
Study locations

Study Summary

The purpose of this study is to evaluate the safety and feasibility of transcutaneous auricular Vagus Nerve Stimulation (taVNS) paired with upper-limb rehabilitation in adults with tetraplegia caused by cervical spinal cord injury.

Interventions

  • DEVICE Transcutaneous Auricular Vagus Nerve Stimulation (taVNS)

Study Locations (2)

Texas

  • Neurorecovery Research Center, TIRR MHH - Houston
  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2025-08-15
Est. Completion 2027-12-30
Phase NA

What the Registry Record Tells You About NCT06543277

The ClinicalTrials.gov registry entry for NCT06543277 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Chronic Incomplete Cervical Spinal Cord Injury (SCI) appearing as the primary indexed condition, and to 1 intervention - of which Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) is the first listed.

NCT06543277 reports 2 study locations spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT06543277 about?

NCT06543277 is a clinical study titled "Safety and Feasibility of Paired Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) With Upper Limb Rehabilitation in Incomplete Spinal Cord Injury". The purpose of this study is to evaluate the safety and feasibility of transcutaneous auricular Vagus Nerve Stimulation (taVNS) paired with upper-limb rehabilitation in adults with tetraplegia caused by cervical spinal cord injury.

What is the current status of trial NCT06543277?

This trial is currently recruiting. It is a NA study. The enrollment target is 12 participants. The study started on 2025-08-15. Estimated completion is 2027-12-30.

What conditions does trial NCT06543277 study?

This clinical trial studies the following conditions: Chronic Incomplete Cervical Spinal Cord Injury (SCI).

What interventions are being tested in trial NCT06543277?

The interventions under investigation include: Transcutaneous Auricular Vagus Nerve Stimulation (taVNS) (DEVICE).

Who is sponsoring clinical trial NCT06543277?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06543277 being conducted?

This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.