iFR Guided Coronary Artery Bypass Grafting Surgery

Recruiting Observational Study
Ischaemic Heart Disease Coronary Artery Disease Coronary Stenosis
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
25 – 80
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
Prakash Punjabi · Other
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About This Trial
The expected outcome of better and improved patency of bypass grafts and its direct relation to pre-operative iFR measurements of stenosis as compared to direct visual physiology of stenosis in the coronary angiogram. To establish the correlation between the use of intracoronary physiology and improved graft patency at 12 months for patients undergoing CABG surgery. It is a minimum of 28 and a m…
Trial Locations
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Eligibility Criteria
INCLUSION CRITERIA 1. Age of 25 to 80 years of age 2. Willing to participate and able to understand, read and sign the informed consent form (ICF) before standard of care elective CABG surgery 3. Undergoing isolated first-time elective CABG surgery 4. Available pre-operative angiography data with i…
Contacts

Prakash P Punjabi, MBBS,MCh,FRCS,FFST,FESC,FCCP

020 3313 2026

P.Punjabi@imperial.ac.uk

CONTACT

Panagiotis G Kyriazis, BSc, MRes

020 3313 2026

Panagiotis.Kyriazis@nhs.net

CONTACT