AI-POD Clinical Validation Study for Obese Patients

University Hospital Bonn (UKB)

Status

Enrolling

Conditions

Acute Cardiovascular Disease

Treatments

Other: Non Interventional

Study type

Observational

Funder types

Other

Identifiers

NCT06595134

310/23-EP

Details and patient eligibility

About

The study is aimed at patients who suffer from severe obesity and receive a computerised tomography (CT) scan of the heart. A total of 1200 patients across Europe are to take part in the study. It is a multi-centre, controlled, open, randomised study. As part of the study, a citizen app will be installed on a smartphone for randomly selected study participants. A fitness tracker will also be issued so that certain parameters, such as heart rate and daily number of steps, can be recorded.

Full description

The clinical validation study of the AI-POD instruments (risk score, CDSS, Citizen App) is designed as a prospective, multicentre observational study. Obese patients (BMI >30 kg/m2) with suspected CVD who are scheduled for a cardiac CT scan (consisting of calcium scoring and coronary CT angiography) will be included in the study. This clinically indicated cardiac CT scan will serve as a baseline examination, and a second cardiac CT scan will be performed after a follow-up period of 2 years. Both cardiac CT examinations will be performed on a photon-counting CT system (PCCT). In addition to the CT data, clinical data (anthropometry and physical parameters such as body weight, height, age, gender, BMI, waist circumference, waist-to-hip ratio, body impedance analysis, cardiovascular risk factors, medication, previous interventions and operations) will be collected, symptoms and results of echocardiography to determine left ventricular function) as well as laboratory data on (subclinical) inflammation (hsCRP, leukocytes, monocyte activation), lipid disorders (HDL, LDL, total cholesterol, triacylglycerides), glucose homeostasis (HbA1c, fasting glucose, HOMA index), liver and kidney function (creatinine, GFR, GOT/ALAT, GPT/ASAT) are collected at a total of 5 visits over 2 years. Half of all included patients will also be randomised to receive access to the Citizen app and a separate fitness tracker device to record the following data: Activity data such as step count, heart rate, height, weight, gender, age, waist circumference circumference, nutritional data such as calorie intake, nicotine, alcohol, sleep.

Enrollment

1,200 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age greater than or equal to 45 years at the time of signing informed consent
BMI greater than or equal to 30 kg/m2
Patients with suspected CVD (>15% pretest probability [ESC guidelines]), referred for cardiac CT examinations (consisting of coronary calcium scoring and coronary CT angiography)
Informed consent of the patient

Exclusion criteria

Any of the following CV conditions within 2 months prior to study inclusion: myocardial infarction, stroke,
Hospitalization for unstable angina pectoris or transient ischemic attack or due to congestive heart failure.
Planned coronary, carotid, or peripheral artery revascularisation known on the day of inclusion
Presently classified NYHA IV heart failure
Having uncontrolled diabetes mellitus (HbA1c ≥ 11%) at day of inclusion
Having uncontrolled hypertension (SBP ≥ 160 mmHg and/or DBP ≥ 100 mmHg) as measured at inclusion
Having severe renal impairment measured as an eGFR < 30 mL/min/1.73 m2 at inclusion
Alanine aminotransferase (ALT) or alkaline phosphatase (APT) level < 3.0 x the upper limit of normal (ULN)for the reference range
Total bilirubin level >1.5 x the ULN for the reference range
History of an active or untreated malignancy or are in remission from a clinically significant malignancy for less than 5 years
Previous organ transplantation or awaiting an organ transplant
Pregnancy or breastfeeding