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Clinical Trial Summary

The aim of the study is to compare different devices available to measure fractional flow reserve (FFR) in coronary arteries.


Clinical Trial Description

The decision to perform a percutaneous coronary intervention (PCI) is usually based on angiographic results alone. Angiography can be used for the visual evaluation of the inner diameter of a vessel. Visual evaluation is limited by inter-individual variability.

Fractional flow reserve provides a functional evaluation, by measuring the pressure decline caused by a vessel narrowing.

The original studies validating the use of FFR were conducted with only one device (St-Jude Medical®). Recently, new FFR devices have been commercialized but have not yet been compared. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03052803
Study type Observational
Source University Hospital, Caen
Contact
Status Completed
Phase N/A
Start date February 1, 2017
Completion date December 1, 2017

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