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NCT Number: NCT07147725

Pulmonary Arterial Hypertension and Associated Cardiovascular Disease Detection Using Artificial Intelligence

Cardiovascular disease (CVD) is a leading global cause of morbidity and mortality and excessive healthcare expenditures. Pulmonary hypertension (PH) represents an insidious and progressive subset of CVD affecting an estimated 1% of the general population, increasing to up to 10% in the population over the age of 65. Recent advancements in artificial intelligence (AI) have shown promise in transforming PH diagnosis by enabling the analysis of complex physiological data. Specifically, AI algorithms applied to electrocardiography (ECG) and phonocardiography (PCG) waveforms captured through novel medical devices, such as smart stethoscopes, have demonstrated potential in detecting PH and other cardiovascular conditions with high sensitivity and specificity.

Despite the promising capabilities of AI algorithms, a significant barrier to their clinical implementation is the lack of high-quality, prospectively collected datasets for validation. Many existing AI algorithms have been trained on retrospective data, which may not capture the variability and complexity of real-world clinical scenarios. This limitation raises concerns about the generalisability and reliability of AI predictions across diverse patient populations.

Therefore, there is a critical need for prospective validation studies to assess the performance of AI algorithms in realworld settings, ensuring their accuracy and applicability before widespread clinical deployment. Imperial College London's Health Impact Lab (Hi Lab) and collaborators continue to develop artificial intelligence (AI) algorithms that use cardiac waveforms to predict cardiovascular disease (CVD), including pulmonary hypertension (PH). The performance of these algorithms requires validation on prospectively collected patient data (waveforms) - where the ground truth for the algorithms under investigation is recorded during routine echocardiography as part of clinical care. This study aims to prospectively collect a large dataset of cardiovascular ECG and PCG data, along with corresponding gold-standard echocardiography findings. This dataset will be used to validate AI algorithms for important CVD, such as pulmonary hypertension enhancing their reliability and clinical applicability.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

This prospective observational cohort and validation study aims to create a patient dataset of point-of-care cardiovascular waveforms for validation of Imperial College London artificial intelligence (AI) algorithms trained for the detection of cardiovascular disease (CVD), using said waveforms as input, with a focus on pulmonary hypertension (PH).

The study will recruit 1,000 unselected patients attending Imperial College Healthcare NHS Trust for routine echocardiography. Each patient will undergo a non-invasive examination using a smart stethoscope that records 3- lead electrocardiogram (ECG) and phonocardiogram (PCG) waveforms, in addition to the standard echocardiography parameters. Baseline demographic data and medical history will also be collected, and a chart review will be performed at 24 months to capture any subsequent morbidity or mortality. The study will validate the AI algorithms by comparing their performance to echocardiography results, the current gold standard for CVD diagnosis. The primary outcome measures will include performance characteristics - sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and F-1 Score of the AI algorithm in detecting CVD.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18 years or above
  • Able to give informed consent
  • Attending for echocardiography at Imperial College NHS Trust

Exclusion criteria

  • Any chest wound, skin pathology or other feature that would prohibit routine stethoscope examination

Treatment and study plan

AI Stethoscope

Device

Patients attending routine echocardiography who satisfy the inclusion and exclusion criteria will be approached before their echocardiography appointment to obtain informed consent to participate in the study. On providing informed consent, each patient will receive a non-invasive, external examination with a smart stethoscope that records a 3-lead electrocardiogram (ECG) and phonocardiogram (PCG) waveforms. This examination will require only one study visit (during routine echocardiography) and no additional visits. The stethoscope is a fully CE-marked device.

In addition to echocardiography parameters and smart stethoscope waveforms, baseline demographics, clinical and medication history will be recorded. These data points will be re-examined at 24 months following enrolment (via chart review).

Primary outcomes

  1. Performance characteristics for developed algorithms

    Time frame: 24 months

    Performance characteristics for developed algorithms (external validation). Performance characteristics include area under the receiver operating characteristic curve (AUROC), sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), positive likelihood ratio, negative likelihood ratio and and F1 Score of the AI algorithm in detecting the condition of interest e.g. PH, compared to echocardiography (ground truth).

Study contacts

Contact information is provided by the study sponsor or research team.

Patrik Bächtiger, MD

CONTACT

[email protected]

Saloni Nakhare, MBChB, MSc

CONTACT

[email protected]

Email

Sponsors and collaborators

Lead sponsor

Imperial College London

Other

Collaborators

  • Imperial College Healthcare NHS Trust

Registry information

Acronym: PULSAR

Important dates

Study start
2025
Primary completion
2025
Study completion
2027
First posted
Aug 29, 2025
Registry last updated
Sep 23, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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