Current partner codePEPTIDESDE
NCT03866148·Not applicable·INTERVENTIONAL

Obstructive Sleep Apnoea and Cardiac Arrhythmias

Status

Unknown

Phase

Not applicable

Enrollment

200

Locations

1

Results

Not posted

Publications

4

Study summary

What the protocol is testing.

This study is a prevelance trial looking at how sleep apnoea affects the heart especially heart rhythms. Previous research shows that patients suffering from sleep apnoea are much more likely to get heart disease and abnormal heart rhythms (arrhythmias). These defects are sometimes missed by the traditional methods of monitoring i.e. 24-hour Holter monitor and ECGs. This means potentially dangerous arrhythmias may not be detected. Additionally, standard therapy for sleep apnoea does not significantly reduce the risk of heart disease. This study will recruit 200 participants over a period of 18 months. The research team will observe the heart rhythms of sleep apnoea patients by inserting an implantable loop recorder (ILR) in up to 100 participants. The other 100 patients will simply have standard care. This device will monitor the heart continuously for 3 years allowing us to detect abnormal heart rhythms and treat as necessary. Demonstrating the incidence of arrhythmia can lead onto a larger study which may change future sleep apnoea management improving their cardiovascular outcomes. Other markers of heart disease such as; blood tests, Magnetocardiography and Echocardiography will be performed on participants to shed more light on the mechanisms which link sleep apnoea and heart disease/arrhythmia.

Full detailed description

Sleep apnoea affects up to 1.5 million adults in the United Kingdom (UK). This puts this population at risk of reduced oxygen levels during sleep, poor sleep and increased breathing effort . All of the above put stress on the body and are proven to increase the risk of high blood pressure, heart failure and vascular problems. This can lead to strokes, heart disease and death. Sleep apnoea patients are at much higher risk of abnormal heart rhythms. Even with continuous positive airways pressure (CPAP) treatment (which is the mainstay in sleep apnoea and does help to reduce arrhythmias) patients are still at higher risk of heart disease and stroke. An implantable loop recorder (Reveal-LINQ) inserted into sleep apnoea patients will be able to continuously monitor a patient's heart rhythm. This will determine the incidence of arrhythmia in sleep apnoea patients. Any significant abnormalities in either arm of the study will be treated as per National Health Service guidelines and best care. The cost associated with this method of intervention will also be considered. If there is a high prevalence of arrhythmia a future larger trial, involving much larger numbers and multiple centres, could be conducted to demonstrate reduced risk of stroke or heart attack using this method of arrhythmia detection and management. Cardiovascular biomarkers, cardiac function, autonomic function and magnetocardiography in these patients could shed light on the mechanisms which cause increased cardiovascular morbidity and mortality.

Interventions

Treatment arms and agents.

DEVICE

Reveal LINQ

Insertion of monitoring device called Reveal-LINQ (an implantable loop recorder)

Timeline

From registration to results.

  1. First posted

    Mar 7, 2019

  2. Study start

    Oct 3, 2019

  3. Primary completion

    Apr 15, 2023

  4. Study completion

    Apr 15, 2025

  5. Results posted

    Not reported

  6. Registry updated

    Jun 18, 2024

Outcomes

What the study measures.

Primary outcomes

Incidence of arrhythmia

Time frame · 3 years

Incidence of arrhythmia in sleep apnoea patients as recorded by ILR vs a no ILR group

Autonomic function before and after CPAP

Time frame · 3 years

Assess the changes to the heart in sleep apnoea patients before and after CPAP in terms of heart rate variability as measured on 24 hour holter monitors. The raw data is taken from the monitor and then analysed manually. The first data set will be from baseline studies which will be compared to studies done at the 1 year follow-up.

Secondary outcomes

Onset and frequency of atrial fibrillation

Time frame · 3 years

Explore the onset and frequency of atrial fibrillation in sleep apnoea patients in order to determine what method of detection is efficient and cost effective.

Rate of Cardiovascular Morbidity

Time frame · 3 years

Explore the impact of inserting an ILR in patients with sleep apnoea on cardiovascular morbidity (stroke and myocardial infarction) compared to those without ILR

Rate of Cardiovascular Mortality

Time frame · 3 years

Explore the impact of inserting an ILR in patients with sleep apnoea on cardiovascular mortality (stroke and/or myocardial infarction resulting in death) compared to those without ILR

Cardiovascular biomarkers before and after CPAP

Time frame · 3 years

Explore the changes to the heart in sleep apnoea patients before and after CPAP in terms of vascular biomarkers - high sensitivity C-Reactive Protein, high sensitivity Troponin-T, N-terminal pro B-type Natriuretic Peptide, Tumour Necrosis Factor-alpha, Matrix Metalloproteinase-9, Interleukin-6, Fibroblast Growth Factor-23. The first data set will be from baseline studies which will be compared to studies done at the 1 year follow-up.

Echocardiography before and after CPAP

Time frame · 3 years

Explore the changes to the heart in sleep apnoea patients before and after CPAP in terms of echocardiogram measures.

Quality of life: EQ-5D-5L questionnaire

Time frame · 3 years

Quality of life measures before and after CPAP as measured by the EQ-5D 5 level questionnaire. This measures various quality of life points from a scale of 1-5. 1 represents poor quality of life and 5 represents good quality of life for each factor. This data will be analysed as per the EuroQol algorithm. The first data set will be from baseline studies which will be compared to studies done at the 1 year follow-up.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
75 Years
Sex
ALL
Healthy volunteers
No

Inclusion Criteria: * Patients with moderate to severe sleep apnoea who require CPAP as standard care (AHI \>15) * Patients between the age of 18 and 75 Exclusion Criteria: * Patients with a diagnosis of atrial fibrillation (AF), atrial flutter and/or ventricular tachycardia (VT) * Patients with an ILR already in-situ or an established indication for ILR * Patients with a palliative diagnosis i.e. life expectancy less than 3 years * Patients who lack capacity

Study locations

1 registered sites.

United Kingdom. Showing up to 24 locations stored in the fast local snapshot.

University Hospital Coventry & Warwickshire

Coventry, United Kingdom

Publications

Results and literature.

Primary links

Continue at the source.

Related trials

More studies on Nesiritide.

Related PeptideStat pages

Put the record in context.

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