Status:
UNKNOWN
Usefulness of the Use of Co-registration Strategy With iFR in Long and/or Diffuse Coronary Lesions
Lead Sponsor:
Maimónides Biomedical Research Institute of Córdoba
Conditions:
Instantaneous Wave Free Ratio
Diffuse Coronary Artery Disease
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Randomized controlled trial to determinate if the physiological iFR pullback evaluation with Syncvision software (intervention group) could be useful in the reduction of stent length implanted, with t...
Detailed Description
Physiological coronary lesion evaluation is actually a routine practice in the labs to guide percutaneous coronary intervention decision making. Unlike FFR, the new index permit us to perform an analy...
Eligibility Criteria
Inclusion
- Age higher than 18 years old.
- Sign of inform consent
- Patients with at least a vessel with angiographic significant lesion (long/sequential or diffuse lesion) \>/= 25 mm of length where the percutaneous strategy is going to be the choice strategy.
- Patients with stable angina, NSTEMI or STEMI (non culprit vessel)
Exclusion
- Patients with Acute Coronary Syndrome with non optimal result of culprit vessel (final TIMI flow \< TIMI III, non-reflow phenomenon during the treatment, residual coronary dissection, lost or compromise of significant side branch).
- Acute Coronary Syndrome and Left Ventricular Ejection Fraction lower than 45%.
- Live expectancy lower than 12 months.
- Patients with severe aortic stenosis.
- Contraindication for dual anti platelet therapy during at least 12 months.
- Patients with indication of bypass surgery in base to Heart Team decision.
Key Trial Info
Start Date :
February 11 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 24 2024
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT04283734
Start Date
February 11 2020
End Date
January 24 2024
Last Update
October 2 2023
Active Locations (1)
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1
Hospital Universitario Reina Sofía
Córdoba, Spain, 14004