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Trial to Compare FFR Measurement With a Non-Side-Hole Guide Catheter Vs. a Side-Hole Guide Catheter

Not Applicable
Completed
Conditions
Coronary Artery Disease
Interventions
Other: FFR Measurement
Registration Number
NCT02480569
Lead Sponsor
North Texas Veterans Healthcare System
Brief Summary

The investigators propose a single center prospective study that will assess two different strategies for measuring Fractional Flow Reserve (FFR) in patients undergoing clinically-indicated coronary angiography in whom FFR measurement is indicated. FFR will be measured with a non-side hole guide catheter (with the guide catheter both engaged and disengaged from the coronary ostium) and with a side-hole guide catheter (with the guide catheter both engaged and disengaged from the coronary ostium) to determine, whether measurements obtained with an engaged side-hole guide catheter are more accurate as compared with those obtained with the engaged non-side hole catheter.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
25
Inclusion Criteria
  • Undergoing a clinically indicated coronary catheterization
  • Need FFR of a coronary artery lesion
  • Agree to participate and able to provide informed consent
Exclusion Criteria
  • Significant difficulty advancing the pressure measuring guidewire into the coronary artery
  • Severe chronic obstructive pulmonary disease
  • Severe ostial disease (>70% diameter stenosis within 5 mm from the coronary artery ostium)

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Side-Hole CatheterFFR Measurement2 FFR measurements from an engaged side-hole guide catheter and a disengaged side-hole guide catheter
Non-Side-Hole CatheterFFR Measurement2 FFR measurements from an engaged non-side-hole guide catheter and a disengaged non-side-hole guide catheter
Primary Outcome Measures
NameTimeMethod
FFR measurement using a guide catheter with and without side holesLess than 1 hour during the coronary angiography
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Dallas VA Medical Center

🇺🇸

Dallas, Texas, United States

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