- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03046823
Imaging-based Diagnosis of Diffuse Coronary Artery Disease and Quantification of Cardiac Remodeling in Obesity
The study aims to:
- Characterize coronary artery disease (CAD) using CT Angiography (CTA) and scaling power law in 100 patients with obesity
- Characterize cardiac remodeling using curvedness-based MRI in 100 patients with obesity
- Compare the differences of cardiac and vascular remodeling in patients with metabolic syndrome and those without
Study Overview
Status
Conditions
Detailed Description
Background and Objectives:
Obesity is a common [affecting about 33% in the general adult population in US] metabolic disorder and it is increasing in prevalence in Singapore (about 10% of general adult population). As obesity is associated with cardiovascular disease (i.e., diffused coronary artery disease, DCAD) and leads to heart remodeling and heart failure, timely and accurate diagnosis of diffused coronary artery disease and its related cardiac remodeling in obesity is clinically urgently needed and this study aims to:
- Characterize coronary artery disease (CAD) using CTA and scaling power law in 100 patients with obesity
- Characterize cardiac remodeling using curvedness-based MRI in 100 patients with obesity
- Compare the differences of cardiac and vascular remodeling in patients with metabolic syndrome and those without
Methodologies: 100 patients with obesity will be recruited for this study. All recruited patients will undergo fasting blood test for diagnosing metabolic syndrome. After that, they will undergo CTA and MRI within 1-2 weeks in-between. Patients' CTA images will be segmented and transformed to build 3D coronary artery models. The application of novel scaling power laws on these models will be used to diagnose diffuse CAD. Based on patients MRI images, the cardiac remodeling will be assessed with a novel curvedness-based imaging analysis method. The differences of cardiac and vascular remodeling in patients with metabolic syndrome and those without will be compared and analyzed.
In addition, subjects shall undergo ultrasound examination of the heart (echocardiogram), carotids and forearm arteries. Doppler and tissue-Doppler echocardiography constitutes the gold standard for cardiac diastolic function assessment. The findings shall be correlated with diastolic cine MRI findings. Carotid and forearm artery ultrasound allows investigation of vessel distensibility, carotid intimal thickness, pulse wave velocity, central arterial blood pressure estimation as well as endothelial function (via flow-mediated dilation). Perturbations of these parameters may be correlated with functional abnormalities on cardiac MRI and coronary disease on CT.
Subjects shall undergo fasting blood tests for metabolic profiling. The tests include blood levels of creatinine, electrolytes, insulin, glycated haemoglobin, fasting lipids, fasting sugar and postprandial sugar (75 g standard oral glucose load). Additionally blood samples shall be stored for potential future studies.
Clinical Significance: If success, this study in obesity should advance understanding of obesity-related CAD and cardiac and vessel remodeling, and further translate into improved diagnosis and treatment in obese patients.
Clinical Significance: If success, this study in obesity should advance understanding of obesity-related CAD and cardiac remodeling, and further translate into improved diagnosis and treatment in obese patients.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Singapore, Singapore, 169609
- National Heart Centre
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Aged 21-80.
- with obesity BMI ≥27 .
- Written informed consent obtained
Exclusion Criteria:
- Individuals unable to provide informed consent.
- Non-cardiac illness with life expectancy <2 years.
- Pregnant state.
- Allergy to iodinated contrast.
- Significant arrhythmia; heart rate ≥ 100 beats/min; systolic blood pressure ≤90 mmHg.
- Renal dysfunction (Glomerular filtration rate (GFR) <45 mL/min/1.73m2).
- Contraindication to beta blockers or nitroglycerin.
- Canadian Cardiovascular Society class IV angina.
- with Cardiac pacemaker
- with brain aneurysm or clips
- with Electronic implants or prosthesis
- with Eye metal foreign body injury
- Severe claustrophobia
- Thyroid dysfunction
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnosis of diffuse coronary artery disease using imaging techniques and quantification of cardiac remodeling in obesity
Time Frame: 36 months
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Imaging-based techniques used are MRI, CTA and Echocardiogram.
Fasting blood tests will be carried out to determine metabolic syndrome.
Cardiac and vascular remodeling in participants with metabolic syndrome and those without will be compared and analyzed.
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36 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: RU SAN TAN, National Heart Centre
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2014/501/C
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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