ClaudicationNCT06176898
Neurostimulation in Intermittent Claudication
A study testing Neurostimulating device in people with Claudication, run by The Leeds Teaching Hospitals NHS Trust at 1 site in United Kingdom.
Trial 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. Read more about this study
- Who is it for?
- Ages 50 to 90 years
- Conditions the study is for
- Claudication
- What is being tested?
- Neurostimulating device
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 16 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 26 Jun 2023to 31 Dec 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
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 50 to 90 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- • Rutherford b/c intermittent claudication with stable symptoms for 6 months with a decision not to undergo any revascularization.
Who cannot join
- • 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
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site, 1 recruiting
- Recruiting
Leeds Teaching Hospitals NHS Trust
Leeds, LS9 7TF
Sarah Hall, 0113 2060460, sarah.hall50@nhs.net
About this study
Official title: The Effect of Neurostimulation on Patient Relevant Outcomes in Patients With Intermittent Claudication: a Pilot Study
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.
- Conditions
- Claudication
- Being tested
- Neurostimulating device
- Keywords
- Vascular Medicine
- Medical subject headings
- Intermittent Claudication
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Neurostimulating deviceDevice
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
| Study group | Role | What they receive |
|---|---|---|
| Neurostimulating device. | Experimental | Not described Receives: Device: Neurostimulating device |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maximal walking distance determined from the six-minute walk test
Maximal walking distance determined from the six-minute walk test (6MWT)
Measured: At baseline and at 8 weeks
Secondary outcomes (2)
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
Measured: At baseline and at 8 weeks
Patient acceptance of the neurostimulator device
Patient acceptance of the neurostimulator device using questionnaire
Measured: At baseline and at 8 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Dec 2023
- Study start26 Jun 2023
- Primary completion31 Dec 2023 (estimated)
- Study completion31 Dec 2023 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ClaudicationStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 16 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Leeds Teaching Hospitals NHS Trust
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06176898
- Sponsor's protocol ID
- VS22/153016
- Status last verified
- Dec 2023
- First submitted
- 26 Sep 2023
- Last updated
- 20 Dec 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 20 Dec 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Neurostimulation on Patient Relevant Outcomes in Patients With Intermittent Claudication: a Pilot Study
- ClinicalTrials.gov ID
- NCT06176898
- Acronym / sponsor ID
- VS22/153016
- Conditions
- Claudication
- Keywords
- Vascular Medicine
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 16 participants (estimated)
- Lead sponsor
- The Leeds Teaching Hospitals NHS TrustUniversity, hospital or other
- Study start
- 26 Jun 2023 (actual)
- Primary completion
- 31 Dec 2023 (estimated)
- Study completion
- 31 Dec 2023 (estimated)
- First posted
- 20 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Neurostimulating device. | Experimental | Device: Neurostimulating device |
Who may qualify
- Ages
- 50 to 90 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- • Rutherford b/c intermittent claudication with stable symptoms for 6 months with a decision not to undergo any revascularization.
Key exclusion criteria (4 listed)
- • Critical limb ischaemia
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Neurostimulating deviceA 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 | Device | Neurostimulating device. |
Primary outcome
Maximal walking distance determined from the six-minute walk test
Time frame: At baseline and at 8 weeks
Maximal walking distance determined from the six-minute walk test (6MWT)
2 secondary outcomes
Quality of life analysis using both generic and disease specific quality of life
Time frame: At baseline and at 8 weeks
Patient acceptance of the neurostimulator device
Time frame: At baseline and at 8 weeks
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Dec 2023.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Neurostimulating device in people with Claudication, run by The Leeds Teaching Hospitals NHS 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 1 inclusion and 4 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: status not confirmed, as of the sponsor's last update on 20 Dec 2023. 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?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Patrick Coughlin, Yes (0113 392 8160, patrick.coughlin1@nhs.net), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Maximal walking distance determined from the six-minute walk test (time frame: At baseline and at 8 weeks). 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 20 Dec 2023.