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320 Multidetector Computed Tomography Prior to Coronary Artery Bypass Surgery

320 Multidetector Computed Tomography in the Preoperative Assessment for Coronary Artery Bypass Graft Surgery

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01169948
Enrollment
0
Registered
2010-07-26
Start date
2010-06-30
Completion date
Unknown
Last updated
2013-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Disease

Keywords

Coronary disease, Coronary artery bypass, Cardiac surgery, Computed tomography, Coronary angiography

Brief summary

Recent advances in technology have resulted in the development of scanners that can n image the heart arteries within 10 to 20 minutes but without the need for admission to hospital or insertion of catheters. This means that coronary heart disease may be more readily identified (or ruled out) and allow better diagnosis and treatment of patients with symptoms suggesting coronary heart disease. Here, we propose to assess the latest and most powerful scanners to see if it can accurately diagnose the extent of coronary artery disease and facilitate the planning of heart surgery.

Interventions

Computed tomography will be performed using a 320 multidetector computed tomography scanner and may include coronary calcium score, coronary angiography and myocardial perfusion scanning.

Sponsors

University of Edinburgh
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients who have undergone conventional coronary angiography and have been referred for coronary artery bypass surgery or valve replacement

Exclusion criteria

* age less than 18 * pregnancy or breast feeding * inability to undergo computed tomography scanning * inability to give informed consent * severe renal failure (serum creatinine \>250umol/l or estimated glomerular filtration rate \<15ml/min) * known allergy to iodinated contrast

Design outcomes

Primary

MeasureTime frame
Coronary artery stenosis defined qualitatively by trained observers and quantitatively by computer software1 month

Secondary

MeasureTime frame
Myocardial perfusion defects defined qualitatively by trained observers and quantitatively by computer software1 month

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026