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Pressure Guidewire Comparison

Primary Purpose

Coronary Artery Disease, Myocardial Ischemia

Status
Completed
Phase
Phase 4
Locations
Netherlands
Study Type
Interventional
Intervention
FFR-measurement with different pressure guidewires
Sponsored by
Lokien van Nunen
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Coronary Artery Disease focused on measuring Fractional Flow Reserve, Pressure wire, Drift

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18-80 years
  • Scheduled to undergo invasive FFR measurement
  • Coronary artery lesions located in the proximal or mid part of the coronary artery
  • Reference diameter of at least 2.0mm

Exclusion Criteria:

  • Severe aortic valve stenosis
  • known conduction disturbances (second- or third-degree AV block)
  • acute myocardial infarction (CK >1,000 U/L less than 5 days ago)
  • bradycardia (less than 45 beats/min)
  • severe hypotension
  • extremely tortuous or calcified coronary arteries precluding FFR measurement
  • history of severe asthma
  • pregnancy
  • inability to provide informed consent.

Sites / Locations

  • Catharina Hospital

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Wirecath - PressureWire X

Arm Description

Patients will undergo simultaneous FFR measurements with the Wirecath and PressureWire X simultaneously.

Outcomes

Primary Outcome Measures

FFR
To compare the pressure signals measured by the different available pressure guidewires, specifically the FFR value
Hydrostatic error
To assess the occurrence of hydrostatic errors when using sensor-tipped wires
Drift
To assess the occurrence of drift between the different pressure guidewires

Secondary Outcome Measures

Signal quality
To assess signal quality and stability between the different pressure guidewires
Maneuverability
To assess maneuverability and handling of the different pressure guidewires

Full Information

First Posted
March 15, 2021
Last Updated
July 14, 2023
Sponsor
Lokien van Nunen
Collaborators
Cavis Technologies AB
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1. Study Identification

Unique Protocol Identification Number
NCT04802681
Brief Title
Pressure Guidewire Comparison
Official Title
Piezo-electric Versus Open Wire Pressure Guidewires for FFR Measurements: Comparison of Two Commercially Available Pressure Wires
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
December 1, 2021 (Actual)
Primary Completion Date
January 19, 2023 (Actual)
Study Completion Date
January 19, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Lokien van Nunen
Collaborators
Cavis Technologies AB

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fractional flow reserve (FFR) is the current gold standard for correct decision making with respect to revascularization in the catheterization laboratory. FFR is measured by using a pressure guidewire equipped with a pressure sensor, positioned distal to the stenosis under investigation. A newly developed pressure wire using open wire technology has recently become commercially available. The purpose of this study is to evaluate whether the Wirecath pressure guidewire can be used as standard pressure guidewire. The effectiveness of the device will be investigated by comparing Wirecath FFR measurements with the measurements of another regular sensor-tipped pressure guidewires during simultaneous FFR measurements in the same vessel.
Detailed Description
FFR is a lesion-specific pressure-derived index of functional severity, defined as the maximum myocardial blood flow in the presence of an epicardial stenosis compared with the maximum flow in the hypothetical absence of the stenosis. FFR is measured by advancing a pressure guidewire into the coronary artery distal to the lesion under investigation and maintained in that position. Distal coronary pressure (Pd) and aortic pressure (Pa) are measured simultaneously while inducing steady state maximum hyperemia. FFR is defined as the lowest value of Pd/Pa achieved during maximum hyperemia. An FFR value = or < 0.80 indicates the presence of myocardial ischemia and indicates PCI is warranted. Existing 0.014" wires with pressure measurement capabilities have been available for more than 20 years. Improvements have been done over time, but they are still regarded as inferior to ordinary guidewires when it comes to maneuverability and general guidewire properties. This is attributed to the microelectronics that are needed to facilitate the pressure measurements in these wires. These existing wires also have issues with signal stability which is often referred to as 'drift'. Drift is an electronical phenomenon that leads to a slow progressive change in the pressure value over time. a not entirely reliable signal quality. A relatively new pressure guidewire, Wirecath, is an equivalent device to the currently commercially available pressure guidewires. In comparative bench tests it has shown very good maneuverability. Moreover due to the 'open wire' technology (and thus lack of microelectronics throughout the wire), the Wirecath has very stable signal properties and is, according to physical law and bench testing, immune against a hydrostatic error and less affected by drifting of the signal, which are limitations with current pressure guidewires. This study is designed to examine and compare the pressure measurements of two commercially available pressure guidewires (Abbott and Cavis Technologies) by simultaneously measuring FFR in the same coronary artery with two different pressure guidewires.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Myocardial Ischemia
Keywords
Fractional Flow Reserve, Pressure wire, Drift

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Model Description
This study is a prospective single center randomized controlled trial of FFR measurements comparing two commercially available pressure guidewires in consecutive patients undergoing routine FFR measurements in the catheterization laboratory.
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Wirecath - PressureWire X
Arm Type
Other
Arm Description
Patients will undergo simultaneous FFR measurements with the Wirecath and PressureWire X simultaneously.
Intervention Type
Device
Intervention Name(s)
FFR-measurement with different pressure guidewires
Intervention Description
Measuring FFR with different pressure guidewires
Primary Outcome Measure Information:
Title
FFR
Description
To compare the pressure signals measured by the different available pressure guidewires, specifically the FFR value
Time Frame
During catheterization
Title
Hydrostatic error
Description
To assess the occurrence of hydrostatic errors when using sensor-tipped wires
Time Frame
During catheterization
Title
Drift
Description
To assess the occurrence of drift between the different pressure guidewires
Time Frame
During catheterization
Secondary Outcome Measure Information:
Title
Signal quality
Description
To assess signal quality and stability between the different pressure guidewires
Time Frame
During catheterization
Title
Maneuverability
Description
To assess maneuverability and handling of the different pressure guidewires
Time Frame
During catheterization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18-80 years Scheduled to undergo invasive FFR measurement Coronary artery lesions located in the proximal or mid part of the coronary artery Reference diameter of at least 2.0mm Exclusion Criteria: Severe aortic valve stenosis known conduction disturbances (second- or third-degree AV block) acute myocardial infarction (CK >1,000 U/L less than 5 days ago) bradycardia (less than 45 beats/min) severe hypotension extremely tortuous or calcified coronary arteries precluding FFR measurement history of severe asthma pregnancy inability to provide informed consent.
Facility Information:
Facility Name
Catharina Hospital
City
Eindhoven
State/Province
Noord-Brabant
ZIP/Postal Code
5623EJ
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There is no plan to make individual (non-anonymized) participant data available to others.

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Pressure Guidewire Comparison

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