Actively Recruiting
Impact of Aortic Valve Disease and Thoracic Aortic Aneurysm on Kinocardiographic Signals
Led by Université Libre de Bruxelles · Updated on 2026-05-01
180
Participants Needed
1
Research Sites
12 weeks
Total Duration
On this page
Sponsors
U
Université Libre de Bruxelles
Lead Sponsor
E
Erasme University Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are exploring kinocardiography (KCG), a portable technique that measures heart mechanical activity by detecting vibrations from heartbeats on the body surface. This study aims to understand KCG signal changes in patients with aortic valve disease (AVD) or thoracic aortic aneurysm (TAA) and to assess if smartphones can help diagnose these conditions. The study compares KCG signals with echocardiography, cardiac MRI, phonocardiography (PCG), and video recordings in affected patients and healthy individuals. Participants include patients with severe AVD or TAA scheduled for interventional treatment, those with varying severities of AVD, and healthy controls matched by age, sex, body surface area, and heart function. After clinical imaging (echocardiography or MRI), researchers record KCG and PCG data using sensors on the chest and back and perform similar measurements with a smartphone. Video recordings are taken alongside KCG signals. For patients undergoing surgery, post-operative KCG and imaging measurements are also collected. Participants will attend sessions coinciding with their clinical imaging appointments, during which multiple recordings (KCG, PCG, video) are made. Researchers will analyze these data to understand KCG signal modifications related to AVD and TAA, comparing them with clinical assessments. The study also evaluates the potential of smartphone-based measurements for diagnosis. The main outcome is to clarify the mechanisms behind KCG changes over 12 months, with additional assessments over 18 months.
CONDITIONS
Brief Title
Aortopathy Relationship To Imagery and Kinocardiography Features (ARTIK)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults over 18 years old
- For interventional treatment group: severe aortic valve disease and/or severe thoracic aortic aneurysm with planned treatment decided by Heart Team
- For aortic valve disease group: aortic stenosis, aortic regurgitation, or bicuspidy confirmed by echocardiography or cardiac MRI
- For control group: adults over 18 years matched by age, sex, body surface area, and left ventricular ejection fraction with other groups
You will not qualify if you...
- Presence of severe heart rhythm disorders such as frequent ventricular extrasystoles or atrial tachyarrhythmias
- Inability to give informed consent
- Subjects with aortic valve disease or thoracic aortic aneurysm excluded from the control group
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Single day
Participants undergo echocardiography and/or cardiac MRI, followed by kinocardiography (KCG), phonocardiography (PCG), smartphone measurements, and video recordings to assess aortic valve disease and thoracic aortic aneurysm.
1 visit (in-person)
Duration - Up to 18 months
Participants are observed over time to understand the changes in kinocardiographic signals and clinical outcomes related to aortic valve disease and thoracic aortic aneurysm.
Follow-up visits as per clinical management
Duration - Immediately post-operative period
For participants undergoing aortic valve replacement or thoracic aortic aneurysm surgery, kinocardiography measurements are performed post-operatively following cardiac MRI and/or echocardiography.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Erasme hospital
Brussels, Belgium, 1070
Actively Recruiting
Research Team
E
Elza Abdessater, MD
P
Philippe van de Borne, MD, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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