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Defining the Diagnostic Value of High-Pitch CCTA and Dynamic CT Perfusion in patients with prior PCI for the Diagnosis of Myocardial Ischemia as Defined by Invasive Flow and Pressure Indices - The PACIFIC-III trial

Defining the Diagnostic Value of High-Pitch CCTA and Dynamic CT Perfusion in patients with prior PCI for the Diagnosis of Myocardial Ischemia as Defined by Invasive Flow and Pressure Indices - The PACIFIC-III trial - The PACIFIC-III trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON50843
Enrollment
140
Registered
2021-06-22
Start date
2021-11-01
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

arteriosclerosis Coronary artery disease

Interventions

None listed

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - History of PCI for stable CAD - Referred for a diagnostic ICA. - Age above 35 years.

Exclusion criteria

Exclusion criteria: - History of severe COPD or chronic asthma - Pregnancy - Renal failure (eGFR

Design outcomes

Primary

MeasureTime frame
To assess the diagnostic performance in terms of sensitivity, specificity, negative predictive value (NPV), positive predictive value (PPV) and diagnostic accuracy of high-pitch CCTA and dynamic CTP for the diagnosis of significant CAD as defined by an FFR

Secondary

MeasureTime frame
(1) To compare the diagnostic capabilities of high pitch CCTA and dynamic CTP to detect significant CAD when defined by instantaneous wave-free ratio (iFR). (2) To investigate the potential of high-pitch CCTA to improve plaque characterization and as such diagnosis of ischemia - due to mounting evidence suggesting a relationship between adverse plaque characteristics and ischemia - and prognosis. (3) To evaluate the prognostic value of high-pitch CCTA and dynamic CTP.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)