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Aortic StenosisISASNCT06826183

Implantable Sensor in Aortic Stenosis

An observational study of Aortic Stenosis, run by Barts & The London NHS Trust at 1 site in United Kingdom.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To establish the relationship between a panel of biological markers obtained from the REVEAL Linq device and exercise performance as judged by cardiopulmonary exercise testing Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Aortic Stenosis
What is being tested?
REVEAL Linq device
Type of treatment
Medical device
How many people
17 participants
Where
1 siteUnited Kingdom
Study dates
15 Aug 2017to 9 Mar 2020
Phase
Observational
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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Asymptomatic severe aortic stenosis

Who may be able to join

  • Severe aortic stenosis defined as effective orifice area (EOA) < 1.0 cm2 (or 0.6 cm2/m2 when indexed for body surface area) and peak velocity > 4.0 m/s or mean gradient > 40mmHg
  • No AS attributable symptoms during clinical consultation
  • Informed consent
  • Aged 18 years of age or over

Who cannot join

  • Left ventricular ejection fraction <50%
  • Severe mitral regurgitation
  • PA systolic pressure >40mmHg
  • Ischaemic heart disease with evidence of ongoing ischaemia
  • Anginal chest pain
  • Inability to cycle
Show all 9Show fewer
  • Unrecordable echo windows
  • Alternative pathology like to be life limiting within 2 years
  • Chronic renal failure (EGFR<30)

Trial locations and contacts

1 site in 1 country.

United Kingdom1 site
  • Barts Health NHS Trust

    London, EC1A 7BE

Other trials in United Kingdom

About this study

Official title: The Use of Activity and Impedance From a Continuous, Implantable Sensor to Detect Deterioration in Asymptomatic Patients With Severe Aortic Stenosis (AS) Under a Watchful Waiting Program

To establish the relationship between a panel of biological markers obtained from the REVEAL Linq device and exercise performance as judged by cardiopulmonary exercise testing

Read the detailed description

Patients with severe aortic stenosis (AS) and symptoms have a poor prognosis without surgical or percutaneous intervention; however patients with severe asymptomatic aortic stenosis can be managed conservatively until the severity worsens to a critical extent. Following these patients up is challenging and inexact, and many methods have been proposed to predict an early deterioration. These include exercise testing, the demonstration of a significant increase in mean gradient across the valve on exercise and biomarkers such as Brain Natriuretic peptide (BNP). Current guidelines suggest that aortic valve surgery should be performed on the basis of symptoms in patients with severe aortic stenosis and even in the absence of symptoms in those with very severe disease. The use of treadmill exercise testing is also advocated to establish the presence of unrecognised symptomatic limitation (Class IIa). The complexity of this process, and the risks posed by severe aortic stenosis with symptoms, lead some authorities recommending surgery on all patients with severe aortic stenosis regardless of symptoms in the presence of evidence of rapid progression.

The burden of aortic stenosis is high in developed countries and increasing because of improved survival and greater longevity. As the population ages the prevalence of disease will become highly significant as moderate or severe AS can be demonstrated in 7% of patients over the age of 75 years, and severe aortic valve (AV) calcification seen in 17-19% of the over 80s. The follow up of these patients is often labour intensive, and variably performed. Consensus statements from the British Heart Valve Society and the European Working Party on Valvular Heart Disease recommend follow up in specialist valve clinics, but contemporary UK data suggest that these are few and far between .

There remains a significant group of patients who die or deteriorate while waiting for interventions and the overall mortality is higher in AS patients than in other forms of heart valve disease. The cause for mortality in patients with AS is believed to be haemodynamic collapse, however a higher rate of symptomless arrhythmic events has been noted in this population including bradyarrhythmias, atrial fibrillation and ventricular arrhythmias; the total burden being around 17% in TAVI candidates on a single 24 Holter monitor. This is unsurprising as part of the pathological process underlying AS includes fibrosis of the left ventricular and especially the septal myocardium.

The principle methods of assessment for patients with severe aortic stenosis remain a resting echocardiogram and clinical assessment. Asymptomatic patients may also be assessed with an exercise treadmill test. However, there is concern that asymptomatic patients may deteriorate or have events between follow up visits, or that adequate follow up arrangements may be difficult to achieve.

Continuous or implantable biological measurement and monitoring is a well-established concept and has been available on pacing devices and used in routine clinical practice for some years. The factor that has limited the usefulness of automatic detection algorithms for identifying deterioration in heart failure remains the large variability in clinical status from day to day, such that a true deterioration may become lost amongst a large number of minor clinical insignificant daily fluctuations. In aortic stenosis however, the situation is different. The disease has an inexorable progression and the presence of symptoms defines the need for definitive therapy. This therefore presents a different objective for device monitoring which is required to demonstrate clear evidence of progressive deterioration in order to justify definitive therapy, rather than the day to day optimisation of heart failure medication.

Many measurable parameters are associated with deterioration in patients with heart failure including increasing heart rate, deteriorating autonomic function and reduced daily activity. The use of these continuous monitored biological variables both available on the REVEAL and Linq devices can be integrated into a multiparameteric model to describe the clinical deterioration in aortic stenosis. This, coupled to a better description of the presence of arrhythmic events, provides an exciting new opportunity, if validated, to improve the care of these patients and aid clinical decision making during longitudinal follow up.

Conditions
Aortic Stenosis
Being tested
REVEAL Linq device
Keywords
cardiopulmonary exercise testing, biomarker
Medical subject headings
Aortic Valve Stenosis

What participants receive

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

  • REVEAL Linq deviceDevice

    Implantable loop recorder

What is being measured

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

  1. To establish the relationship between a panel of biological markers obtained from the REVEAL Linq device and exercise performance as judged by cardiopulmonary exercise testing.

    Measured: 12 months

  2. The regressive relationship between total weekly activity from the Reveal Linq and change in VO2 peak /Oxygen Uptake Efficiency Slope (OUES) established by cardiopulmonary exercise testing between visits.

    Measured: 12 months

Secondary outcomes (5)
  1. The relationship between weekly heart rate variability and VO2 peak /OUES

    Measured: 12 months

  2. The relationship between weekly heart rate and VO2 peak /OUES

    Measured: 12 months

  3. The relationship between acoustic murmur intensity and VO2 peak /OUES

    Measured: 12 months

  4. The relationship between S1/S2 intensity and VO2 peak/ OUES

    Measured: 12 months

  5. The relationship between murmur intensity augmentation and VO2 peak/OUES

    Measured: 12 months

Timeline

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

  1. First posted13 Feb 2025
  2. Study start15 Aug 2017
  3. Primary completion9 Mar 2019
  4. Study completion9 Mar 2020

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
17 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06826183
Sponsor's protocol ID
011760
Acronym
ISAS
Status last verified
Feb 2025
First submitted
23 Jan 2019
Last updated
13 Feb 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes

Questions about this trial

What is this clinical trial studying?

An observational study of Aortic Stenosis, run by Barts & The London 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 4 inclusion and 9 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: finished, as of the sponsor's last update on 13 Feb 2025. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

To establish the relationship between a panel of biological markers obtained from the REVEAL Linq device and exercise performance as judged by cardiopulmonary exercise testing. (time frame: 12 months). The study lists 2 primary outcomes in all. 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 13 Feb 2025.

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