ClinicalTrials.gg
RecruitingNCT06176898Updated Dec 20, 2023

Neurostimulation in Intermittent Claudication

An interventional study of Neurostimulating device in Claudication, sponsored by The Leeds Teaching Hospitals NHS Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 50 Years to 90 Years. Per ClinicalTrials.gov, last updated 2023-12-20.

Sponsored by The Leeds Teaching Hospitals NHS Trust · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2023, 2 years 10 months ago, but the record still lists the study as recruiting.
  • Registered 3 months after the study started (first participant enrolled Jun 2023, registered Sep 2023).
  • Started Jun 2023; still recruiting 3 years 4 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Not applicable
Ages
50 Years to 90 Years
Sex
All
01

Study summary

Intermittent claudication is a condition where a patient suffers with cramp-like pain experienced in the muscles of the legs (often the calf muscles) brought on by walking and relieved by stopping walking and resting. It is caused by furring of the arteries (atherosclerosis) often referred to as a circulation problem. It has a significant effect on a sufferers' quality of life. However, in 75% of patients with this condition, the leg symptoms will either stay static or improve slightly even with no treatment. The first line treatment is enrolment in an exercise / walking programme but these are not widely available on the NHS. Failing this, minimally invasive treatment - opening up the narrowing of the artery with either a balloon or stent - can be performed but they are not without risk (being an invasive treatment) and the narrowing often reoccurs in time. Due to the benign natural history of the leg, surgery is less frequently being used. This therefore leaves us with a large number of patients with symptoms with no treatment options and thus a poorer quality of life. Neurostimulation has been used to treat a number of neurological conditions. This study will use a specific device that is attached to the outer aspect of the ear to deliver a neurostimulation to a small branch of the Vagus nerve which through nerve pathways that course through the brain is believed to improve the blood supply to the lower legs.

Read the detailed description

Lower limb peripheral arterial disease (PAD) is common, affecting over 200 million people worldwide and present in 12 to 14% of the global population (20% over the age of 75 years)1. The most common symptom is intermittent claudication, a symptom of muscular lower limb pain brought on by exertion and relieved by rest2.

PAD is the third leading cause of atherosclerotic cardiovascular morbidity, following coronary artery disease and stroke, yet the natural history of the limb in patients with IC is relatively benign with 75% of patients finding that symptoms either remain static or are somewhat improved with no treatment2. It is due to this natural history of the limb that there is an increasing tendency to manage patients with claudication conservatively (ie. Non-invasively).

In patients with intermittent claudication, CV prevention and exercise training are the cornerstones of management3. There is good evidence for enrolment of patients into a supervised exercise programme, providing bot improved walking distance and quality of life, yet widespread provision of such programmes are currently not available within the NHS and further are unlikely to be delivered within the coming years4.

Revascularisation has historically been indicated if daily life activity is severely compromised by the lower limb symptoms and such revascularisation is primarily performed endovascularly with balloon angioplasty +/- stent insertion where needed. The ability to perform endovascular revascularisation is determined by the anatomical location and severity of the lower limb atherosclerosis. Endovascular interventions work best with short focal stenoses rather than longer occlusion where surgical revascularisation is the better option2. Such interventions are invasive and carry risks including risk of amputation and so surgical revascularisation is now rarely performed for intermittent claudication. Further, there is now data available that suggests that early invasive revascularisation in patients with claudication may in the longer term increase the risk of major limb amputation. This means that there is a cohort of patients who have significant claudication symptoms affecting their quality of life who are either (i) not offered revasculairsation or (ii) not prepared to accept the risks of major lower limb revascularisation.

Given this, there is a need to explore further non-invasive methods that could enhance walking distances in patients with IC and thus improve overall quality of life and overall cardiovascular fitness without exposing patients to invasive revascularisations.

There has been an increasing focus on the role of neuromodulation in the management of several chronic diseases5. Neuromodulation is defined as a physiological process which consists of the alteration of neuronal and synaptic properties by neurons or substances released by neurons. Neuromodulation, thanks to intrinsic and extrinsic brain feedback loops, seems to be the best way to exploit brain plasticity for therapeutic purposes.

Vasomotion is believed to play a pivotal role in capillary function and microcirculation. Based on spontaneous oscillating change of arteriole and venule diameter it has been theoretically suggested that oscillatory perfusion may be superior to steady-state flow. It has been shown that continuous electrical stimulation of sympathetic nerves induces a tonic vasoconstriction6.

Consistently, procedures like lumbar sympathectomy are used to enhance blood supply in malperfused limbs. Enhanced parasympathetic stimulation may also cause vasodilatation. We hypothesise that auricular vagus stimulation could modulates afferent parasympathetic activity and potentially improves microcirculation7.

From a medical viewpoint, neurostimulation techniques do provide several advantages with respect to conventional drug or invasive surgical treatments:

  • Specificity: stimulation can be targeted to particular areas avoiding the insurgence of systemic side-effects, typical of traditional drug therapies;
  • Safety: neurostimulation techniques are generally well-tolerated and almost devoid of dangerous side effects;
  • Flexibility: the treatment can be interrupted at any time. One such device that allows neurostimulation to be delivered is the DUCEST neurostimulator device. This is a minimally invasive device that stimulates the afferent branches of the vagus nerve situated within the outer aspect of the ear lobe. (Fossa triangularis).

Figure 1: Anatomical landmarks within the ear.

Figure 2: The Ducest Medical device.

Figure 3: The application of the Ducest Medical device to the ear.

One study in the UK has looked at the effect of the DUCEST neurostimulator in 30 patients with the most severe limb ischaemia who had no revascularisation option and has found that were significant improvements in the size of and flow through the calf arteries. This corresponded with an avoidance in major limb amputation in 11 of the 30 patients.

No study in the UK has formally assessed the effect of such an intervention on patients with IC.

There is a large cohort of patient who would potentially benefit from a low risk, non-invasive intervention aimed at increasing walking distances and improving quality of life.

02

Conditions studied

  • Claudication

Keywords

  • Vascular Medicine
03

In context

Intermittent Claudication

309 studies on the registry are indexed under Intermittent Claudication; 46 are open to participants now.

This study's planned enrollment of 16 is below the median of 74 across 242 interventional studies indexed under Intermittent Claudication.

Browse Intermittent Claudication studies →

Lead sponsor

The Leeds Teaching Hospitals NHS Trust is the lead sponsor of 101 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
50 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

    • Rutherford b/c intermittent claudication with stable symptoms for 6 months with a decision not to undergo any revascularization.

Exclusion criteria

Exclusion Criteria:

    • Critical limb ischaemia

      • Previous external ear surgery
      • Patients with either a cochlear implant or a permanent pacemaker / cardiac defibrillator device
      • Significant cardiorespiratory or musculoskeletal disease (as determined by the medical team) that would contraindicate a 6-minute walk test
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
16 participants (estimated)

Study arms

  • Experimental
    Neurostimulating device.

    Device: Neurostimulating device

Interventions

  • DeviceNeurostimulating device

    A trained practitioner will apply the neurostimulator to the patient's ear. The patient will wear the neurostimulator for a period of three week with the position of the neurostimulator moving from one ear to the other on a weekly basis. After 3 weeks the neurostimulator will be removed and the patient will then undergo further clinical assessment at week 8. At the 8 week clinical assessment, the patient will undergo the same assessments, namely: * Six minute walking test (6MWT) * Quality of life assessment using both generic (Short form 12) and disease specific (Vascuqol) questionnaires

06

What researchers measure

Primary outcomes

  1. Maximal walking distance determined from the six-minute walk test

    Maximal walking distance determined from the six-minute walk test (6MWT)

    Time frame: At baseline and at 8 weeks

Secondary outcomes

  1. Quality of life analysis using both generic and disease specific quality of life

    Quality of life analysis using both generic and disease specific quality of life, using quality of life questionnaire

    Time frame: At baseline and at 8 weeks

  2. Patient acceptance of the neurostimulator device

    Patient acceptance of the neurostimulator device using questionnaire

    Time frame: At baseline and at 8 weeks

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 20, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06176898
Responsible party
Sponsor
First posted
Dec 20, 2023
Start date
Jun 26, 2023
Primary completion
Dec 31, 2023 (estimated)
Completion
Dec 31, 2023 (estimated)
Last update
Dec 20, 2023

Study contacts

Patrick Coughlin, Yes
Contact
patrick.coughlin1@nhs.net
0113 392 8160

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion