Registry of Patients That Have Undergone ICA or PCI
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Coronary Artery Disease. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Netherlands
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Registry of Patients That Have Undergone an Invasive Coronary Angiography and/or Percutaneous Coronary Intervention
Overview
In Invasive Coronary Angiography there are multiple invasively obtained measurements to determine the funcitonal significance of Cornary Artery Disease. In this Registry, patients who have undergone Invasive Coronary Angiography or Percutaneous Coronary Intervention are included to investigate diagnostic and prognostic implications of the invasive measurements.
Primary outcome measures
- Fractional Flow Reserve (FFR) [Time frame: Upon inclusion at index procedure]
- Instantaneous wave-free ratio (iFR) [Time frame: Upon inclusion at index procedure]
- Quantitative Flow Ratio (QFR) [Time frame: Upon inclusion at index procedure]
- Stenosis percentage [Time frame: Upon inclusion at index procedure]
Secondary outcome measures (1)
- Major adverse cardiac events, cardiac death or repeat revascularization [Time frame: 5 years]
Eligibility criteria
Inclusion criteria
- 18 years
- Has undergone or will undergo a clinically indicated invasive coronary angiography.
- Has undergone or will undergo a clinically indicated percutaneous coronary intervention.
Exclusion criteria
- Not willing / unable to provide informed consent.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Netherlands · 1 center
- Amsterdam Univeristy Medical centers, location VUmc — Amsterdam
Identifiers
NCT: NCT04815928 · ICA-PI