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NCT07680127 · ClinicalTrials.gov registry record · NA

TENS of Auricular Vagal Nerve for Radiation Necrosis

A NA study, sponsored by Virginia Commonwealth University.

Not yet
Registry status
NA
Development phase
40
Enrollment target

NCT07680127: Clinical Trial NA study, sponsored by Virginia Commonwealth University.

NCT07680127 is a NA study that has not yet begun recruiting, run by Virginia Commonwealth University. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07680127, a NA study, has not yet begun recruiting, sponsored by Virginia Commonwealth University.

NOT YET RECRUITING
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

This is a multi-center, randomized, blinded trial evaluating the effect of transcutaneous auricular vagal nerve stimulator (taVNS) on radiation necrosis-related cerebral edema. In this study, consenting and eligible patients will be assigned to one of two arms: treatment (Arm 1) or sham (Arm 2). Patients in both arms will have imaging performed and tissue and blood collected for assessment of changes in area of contrast enhancement and cerebral edema, inflammatory markers, and markers of blood-brain barrier permeability.

Primary Outcome

Percent change in serum inflammatory marker TNF-alpha utilizing serum inflammatory marker analysis from collected blood samples

Interventions

  • DEVICE Sham
  • DEVICE Transcutaneous auricular vagal nerve stimulation (taVNS)

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2026-07-31
Est. Completion 2029-08-31
Phase NA
Virginia Commonwealth University

558 total trials

What is known before NCT07680127 opens enrollment

NCT07680127 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Sham is the first listed.

NCT07680127 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07680127 about?

NCT07680127 is a clinical study titled "TENS of Auricular Vagal Nerve for Radiation Necrosis". This is a multi-center, randomized, blinded trial evaluating the effect of transcutaneous auricular vagal nerve stimulator (taVNS) on radiation necrosis-related cerebral edema. In this study, consenting and eligible patients will be assigned to one of two arms: treatment (Arm 1) or sham (Arm 2). Pat...

What is the current status of trial NCT07680127?

This trial is currently not yet recruiting. It is a NA study. The enrollment target is 40 participants. The study started on 2026-07-31. Estimated completion is 2029-08-31.

What interventions are being tested in trial NCT07680127?

The interventions under investigation include: Sham (DEVICE), Transcutaneous auricular vagal nerve stimulation (taVNS) (DEVICE).

Who is sponsoring clinical trial NCT07680127?

This trial is sponsored by Virginia Commonwealth University, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07680127's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 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

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Source: ClinicalTrials.gov NCT07680127, the US trial registry maintained by the National Library of Medicine. NCT07680127 (small enrollment · none site footprint · not yet recruiting) retrieved and formatted by PlainTrial, see methodology.