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Transcutaneous Hypoglossal Nerve StimulationZeus-BPVNCT07917260

Assessing Blood Pressure Variability in a Healthy Adult Population During Transcutaneous Hypoglossal Nerve Stimulation With the Zeus Sleep Device

A study testing Zeus Sleep device in people with Transcutaneous Hypoglossal Nerve Stimulation, run by Royal Brompton & Harefield NHS Foundation Trust at 1 site in United Kingdom.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

Transcutaneous hypoglossal nerve stimulation is an emerging treatment option for Obstructive Sleep Apnoea (OSA), a sleep condition where breathing is repeatedly limited. The standard treatment for OSA is not always well tolerated therefore, more alternatives are needed. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Zeus Sleep device
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteUnited Kingdom
Study dates
29 Sep 2026to 29 Mar 2027
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • Adults aged 18 or older
  • Either biological sex
  • Healthy volunteers
  • Able to provide informed consent
  • No contraindications to hypoglossal nerve stimulation using the Zeus device
  • BMI >18.5 and <30kg/m2

Who cannot join

  • Skin allergy, including eczema or allergic contact dermatitis in device placement area
  • Diagnosed heart condition or cardiovascular disease
  • Cardiovascular event in the previous 2 months
  • Implanted medical devices including cardioverter defibrillator and pacemaker
  • Previous or current cardiac arrhythmia
  • Autonomic neuropathy
Show all 21Show fewer
  • Neuromuscular disease
  • Diagnosed epilepsy or recurrent seizures
  • Hypertension (>140/90 mmHg)
  • Hypotension (<95/65 mmHg)
  • Metal work in the head or neck, excluding dental fillings
  • Current migraine
  • Pregnancy
  • Diagnosed or suspected deep vein thrombosis within previous 2 months
  • Recent cancer diagnosis or cancerous legions in proximity to device placement area
  • Alcohol dependence
  • Recent infection requiring hospital admission or medical treatment within the previous month, including leprosy
  • Swollen, inflamed, infected, or broken skin in device placement area
  • Recent surgery within 10 months in, or near, device placement area
  • Currently taking medications, excluding contraceptive medication
  • Long facial hair in device placement area

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Professor Michael Polkey contact

mike.polkey@nhs.net

United Kingdom1 site, 1 recruiting
  • Royal Brompton Hospital

    London, SW3 6NP

    Recruiting

Other trials in United Kingdom

About this study

Transcutaneous hypoglossal nerve stimulation is an emerging treatment option for Obstructive Sleep Apnoea (OSA), a sleep condition where breathing is repeatedly limited. The standard treatment for OSA is not always well tolerated therefore, more alternatives are needed.

Transcutaneous hypoglossal nerve stimulation uses a device, such as Zeus, which sticks underneath the chin to deliver electrical pulses during sleep. These pulses stimulate the hypoglossal nerve to prevent the tongue from relaxing and blocking the airway.

Device placement is important for specific nerve targeting; however, its proximity is close to receptors involved in blood pressure regulation. Whilst current research indicates that transcutaneous stimulation is unlikely to increase blood pressure, OSA patients have an increased risk of developing high blood pressure, therefore treatment options should not make this worse. Further research to understand the impact of transcutaneous hypoglossal nerve stimulation on blood pressure is therefore needed. In this study, the blood pressure of participants will be measured whilst they wear the Zeus sleep device. It is expected that blood pressure will either decrease or remain constant in line with current research. Findings could facilitate improved confidence in device use for OSA treatment and provide patients with alternative treatment options.

Read the detailed description

During sleep the upper-airway muscles relax, in obstructive sleep apnoea (OSA) this causes repeated narrowing (hypopnoea) and obstruction (apnoea) (NICE, 2021). These periods of reduced breathing cause arousals fragmenting sleep. Symptoms include snoring, impaired performance, waking headaches, and excessive daytime sleepiness (Arnardottir et al., 2016, Spicuzza et al., 2015). OSA additionally impacts quality of life and cognition (Vaessen et al., 2015) and increases risks of hypertension and cardiovascular morbidity (Peppard et al., 2000, Nieto, 2000, Marin et al., 2012). Diagnosis of OSA uses sleep studies, requiring an apnoea hypopnoea index (AHI) of ≥5/hr (NICE, 2021). Peppard et al. (2013) estimate the prevalence of sleep disordered breathing, of which OSA is the most common, to be 26% of 30-70-year-olds and rising.

The gold standard treatment of OSA is continuous positive airway pressure (CPAP) (NICE, 2021), requiring >4hrs/night usage for effective treatment and risk reduction; however, CPAP is not always well tolerated. A review by Weaver et al. (2008) found CPAP nonadherence rates of 29-83%. Alternative treatments include positional modifiers, mandibular advancement devices, and surgery (NICE, 2021, Spicuzza et al., 2015) whose usage is limited by pathophysiology. Further CPAP alternatives are needed.

Hypoglossal nerve stimulation (HNS) is an emerging OSA therapy which uses electrical stimulation to contract the genioglossus muscle, preventing prolapse and maintaining airway patency (NICE, 2017). Strollo et al. (2014) conducted a prospective, single-group, cohort study where non-CPAP compliant OSA patients had a subcutaneous HNS device implanted. A clinically significant decrease in median AHI of 68% (29.3 to 7.4/hr, P<0.001) was seen 12 months post-implantation alongside improved sleepiness and quality of life. A separate study of 113 participants by Woodson et al. (2025) also showed significant improvements in mean AHI (-18.3 ± 11.8/hour, P<0.001) following HNS implantation. Whilst HNS has shown promising efficacy and acceptable safety profile (NICE, 2017, Strollo et al., 2014, Woodson et al. 2025, Friedman et al. 2016), HNS requires a general anaesthesia and carries all the associated risks and costs of an invasive procedure. Interest has therefore turned to transcutaneous HNS as a non-invasive, cost-efficient alternative.

According to Steier et al. (2011), transcutaneous electrical stimulation (TESLA) of the hypoglossal nerve via bilateral hydrogel patches located in the submental area causes contraction of the genioglossus muscle similarly to subcutaneous HNS. A recent randomised controlled trial in OSA patients by Ratneswaran et al., (2023) compared TESLA to usual care (CPAP). An adjusted reduction in AHI of 7/hr with TESLA was seen at 3 months, however this was not significant (P=0.12) potentially due to small sample size or absent additional interrogation. Indeed, Pengo et al. (2016) indicated that only some participants are responders to TESLA, in their randomised, sham-controlled crossover trial a significant reduction in AHI was only seen in responders (9.1/hr, p=0.004). Meta-analysis by Wang et al. (2025) and Young Jae Byun et al. (2020) both concluded that TESLA results in a meaningful AHI reduction. TESLA appears to be well tolerated by patients with minimal adverse events (Pengo et al., 2016, Ratneswaran et al., 2023, Reed et al., 2016).

Despite the promising research, it is possible that submental electrical stimulation could affect blood pressure due to its proximity to carotid sinus baroreceptors. A similar device to TESLA, TENS machines, are contraindicated for use in the neck region (NHS, 2017). However, a sham-controlled, randomized crossover trial of HNS in 60 participants by Dedhia et al., (2023) concluded there was not a significant difference in mean 24-systolic blood pressure between sham and active groups. Furthermore, a study by Alsharifi et al. (2023) found submental TESLA in 13 healthy participants caused a significant decrease in blood pressure (systolic: p=4.93E-06, diastolic: p=3.48E-09, mean: p=3.88E-08); supported by a meta-analysis that concluded electrical stimulation of the upper airways reduced both systolic and diastolic blood pressure (Khaled et al., 2025). Whilst current evidence indicates that TESLA is unlikely to elicit hypertension, in a patient cohort already at increased risk of hypertension and cardiovascular morbidity, it is vital risk is not compounded by treatment.

This study aims to evaluate the short-term impact of hypoglossal nerve TESLA on blood pressure. We hypothesise that submental TESLA will not increase blood pressure or short-term blood pressure variability and may lead to modest reductions, consistent with previous studies.

Being tested
Zeus Sleep device

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Zeus Sleep deviceDevice

    Transcutaneous hypoglossal nerve stimulation using the Zeus Sleep device

Study groups in NCT07917260
Study groupRoleWhat they receive
Group 1- Active stimulation followed by sham stimulationExperimentalNot described
Receives: Device: Zeus Sleep device
Group 2- Sham stimulation followed by active stimulationExperimentalNot described
Receives: Device: Zeus Sleep device

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from baseline in systolic and diastolic blood pressure during Zeus sleep device usage

    Measured: baseline, intervention

Secondary outcomes (1)
  1. Change in pulse rate variability from baseline during active stimulation

    Measured: baseline, intervention

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Nov 2026
  2. Study start29 Sep 2026
  3. Primary completion19 Feb 2027 (estimated)
  4. Study completion29 Mar 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07917260
Sponsor's protocol ID
368532
Acronym
Zeus-BPV
Status last verified
Nov 2026
First submitted
25 Sep 2026
Last updated
4 Nov 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

A study testing Zeus Sleep device in people with Transcutaneous Hypoglossal Nerve Stimulation, run by Royal Brompton & Harefield NHS Foundation Trust at 1 site in United Kingdom.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 21 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 4 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Abigail Smart (020 7351 8910 ext. 88910, abigail.smart@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from baseline in systolic and diastolic blood pressure during Zeus sleep device usage (time frame: baseline, intervention). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2026.

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