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Blinding and Adverse Effects of Ultrasonic Vagus Nerve Stimulation (U-VNS) (BLAST)

U

University of Nottingham

Status and phase

Completed
Phase 2
Phase 1

Conditions

U-VNS
Sham U-VNS

Treatments

Device: Ultrasound Vagus Nerve Stimulation (U-VNS)
Device: Sham U-VNS

Study type

Interventional

Funder types

Other

Identifiers

NCT07091812
FMHS 29-1124

Details and patient eligibility

About

The vagus nerve is a large nerve that runs from the gut to the brain. It consists of two main sections, left and right, and comprises a series of branches. One of these branches runs through the ear. Stimulating the vagus nerve with a stimulation device, either implanted in the body or applied to the skin, has been used to treat a number of health conditions associated with the functioning of the vagus nerve. It has also been explored for tinnitus. Tinnitus is the perception of sound in the absence of an external source. It is believed to be related to abnormal activity in the brain. Stimulation of the vagus nerve may be an effective way of normalising this brain activity, thereby reducing tinnitus.

Two types of vagus nerve stimulation (VNS) have been trialled: 1) invasive VNS, using a surgically implanted vagus nerve stimulator and 2) non-invasive VNS, using electrical stimulation devices that are placed on the skin, near a section of the vagus nerve. Past studies of these techniques show that VNS may be a promising future treatment for tinnitus. However, there is not enough data available to draw a firm conclusion on whether VNS is effective at reducing tinnitus or not. Furthermore, all previous studies of VNS for tinnitus have used electrical stimulation of the vagus nerve. Stimulating the vagus nerve, whether through an implanted device or a device on the skin, comes with serious technical challenges. Most importantly, electric currents follow the path of least resistance. When running through biological tissues, such as skin, cartilage or bone, it is difficult to aim for the part of the body that needs to be stimulated. This means it isn't always easy to tell whether the vagus nerve is indeed being stimulated and how much of the current is actually reaching the vagus nerve.

This problem can be overcome by ultrasound stimulation. Ultrasound stimulation employs high frequency sound waves to stimulate tissue. These soundwaves travel through the human body much more predictably than electric currents. As such, ultrasound stimulation of the vagus nerve may be more effective than electrical stimulation. The ZenBud device is designed to apply ultrasound stimulation to part of the vagus nerve that runs through the ear. Ultrasound stimulation allows for more targeted stimulation, increasing the chance of the stimulation reaching the vagus nerve. The ZenBud device is safe for use in healthy adults and received CE marking based on CE assessments conducted at the University of Nottingham Appendix VI-IX).

However, before this device can be used to test whether this approach can reduce tinnitus symptoms, two questions must be answered: Firstly, can people tell whether they're receiving the real VNS or a placebo? Secondly, what are the type, onset and duration of any adverse effects resulting from U-VNS? We know from the testing performed as part of the CE marking that it is safe. However, there may still be mild adverse effects, such as redness, warming up of the skin etc. It is important to understand these mild adverse effects, so that participants can be fully informed.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged 18 or over
  • Good general health
  • Willing and able to provide informed consent
  • Not currently taking any prescribed medication (except contraceptive pill)
  • Able and willing to remove any piercings in the ears

Exclusion criteria

  • Current or past diagnosis of a neurological psychiatric condition
  • Current or past diagnosis of cardiac arrhythmia
  • Use of medication or recreational drugs that affect the nervous system in the past 3 months
  • Currently pregnant
  • Allergy to aquasonic gel or any of its components (propylene glycol, glycerin, isothiazolinones)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

20 participants in 2 patient groups

U-VNS
Experimental group
Description:
Active ultrasound vagus nerve stimulation
Treatment:
Device: Ultrasound Vagus Nerve Stimulation (U-VNS)
Sham
Sham Comparator group
Description:
Sham device indistinguishable from real U-VNS stimulator
Treatment:
Device: Sham U-VNS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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