Coronary Artery Disease Clinical Trial
Official title:
Investigation of the Role of Hemodynamics in Re-stenosis of CABG Patients
NCT number | NCT02791087 |
Other study ID # | 2013/366/C |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | June 2013 |
Est. completion date | October 2018 |
Verified date | September 2017 |
Source | National Heart Centre Singapore |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
CFD simulations in this study provide detailed hemodynamics information, which cannot be obtained from cardiac images alone. The investigators hypothesize that our proposed simulations will provide strong correlation between hemodynamic parameters, such as WSSG and SPA, and clinically identified graft stenosis. These correlations will allow the investigators to identify the future patients at high risk of graft stenosis and lead to future researches on optimizing and refining surgical plans, such as finding optimal proximal and distal anastomoses locations, optimal graft length and diameter, which could lead to improved longevity of the graft. Once CFD coupled shape optimizer is validated, it could be part of the surgical simulator to help in training the next generation physicians. It could provide new viewpoints for assessing whether some modified surgical techniques are better or not. It could also aid in designing and evaluating the vascular medical devices, including stent, artificial graft, and etc., which would lead to better surgical outcome.
Status | Completed |
Enrollment | 54 |
Est. completion date | October 2018 |
Est. primary completion date | October 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Aged 21-80. - Undergoing or underwent CABG with at least one saphenous vein graft. (Only for recruitment of CABG patients) - No known history of coronary artery disease (only for recruitment of volunteers with Stable/unstable angina). 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) <30 mL/min/1.73m2). - Contraindication to beta blockers or nitroglycerin. - Canadian Cardiovascular Society class IV angina. |
Country | Name | City | State |
---|---|---|---|
Singapore | National Heart Centre Singapore | Singapore |
Lead Sponsor | Collaborator |
---|---|
National Heart Centre Singapore |
Singapore,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Evidence of allergic reaction due to CTA scan contrast | Within first day after scan |
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