An Evaluation of a Physiology-guided PCI Optimisation Strategy

Coronary Artery Disease Clinical Trial

— Target-FFR  

Official title:

How Often Can Optimal Post Percutaneous Coronary Intervention (PCI) Fractional Flow Reserve (FFR) Results be Achieved? - a Randomised Controlled Trial of FFR Targeted PCI (the Target FFR Study)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03259815
• Other study ID #: 17/CARD/10
• Secondary ID: IRAS ID 223780
• Status: Completed
• Phase: N/A
• Start date: March 8, 2018
• Est. completion date: December 4, 2020

Study information

• Verified date: March 2022
• Source: NHS National Waiting Times Centre Board
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

There has recently been renewed interest in the measurement of post percutaneous coronary intervention (PCI) Fractional Flow Reserve (FFR). Previous studies have suggested that post-PCI FFR values ≥0.90 are associated with better clinical outcomes for patients but the available data suggest that despite angiographically satisfactory results, this is actually achieved in less than 40% of cases.

The main mechanisms for sub-optimal post-PCI FFR measurements have been proposed to be suboptimal stent deployment, unmasking of a second lesion in the target vessel post PCI, residual diffuse disease in the untreated segments and pressure drift (a technical artefact of pressure wire technology).

Using post-PCI FFR to guide stent optimisation and/or further intervention in the target vessel has been shown to increase the frequency of achieving optimal post-PCI FFR results (and therefore presumably better clinical outcomes). However, there are additional costs involved in the routine use of post-PCI FFR and it is not clear just how often it is even possible to increase the initial post-PCI FFR to ≥0.90. This uncertainty means that it is currently difficult to either recommend the routine use of post-PCI FFR or justify its cost.

The investigators propose a prospective study to assess the feasibility of achieving post-PCI FFR ≥0.90 during standard PCI procedures in consecutive patients. The study would also attempt to elucidate the mechanisms for sub-optimal FFR results when they occur. The investigators anticipate using the data from this developmental study to support a subsequent funding application for a definitive phase 3 study of the impact of FFR targeted PCI on clinical outcomes.

Description:

Original hypothesis

A simple Physiology-guided Incremental Optimisation Strategy (PIOS) can increase the proportion of patients undergoing PCI in whom a post-PCI FFR ≥0.90 can be achieved from 40% to 60%.

Experimental details and design of proposed investigation

Overall aim:

A randomised controlled trial of a physiology-guided optimisation strategy to determine the feasibility of increasing the proportion of post-PCI FFR measurements ≥0.90 in a consecutive series of patients undergoing standard PCI procedures.

Study Population:

260 consecutive patients with stable angina referred for invasive management to the cardiac catheterisation lab who have been selected to undergo PCI based on either angiographic appearances or prior FFR assessment. Patients will be caffeine free for >12 hours pre-procedure.

Methods/Design:

Informed consent will be obtained prior to cardiac catheterisation in all potential subjects conforming to the inclusion and exclusion criteria.

Patients will then be randomised to one of two groups (described below) and PCI will be performed, using a pressure guidewire, according to standard practice at the Golden Jubilee National Hospital (including lesion pre-dilation and post-dilation of the stented segment).

Group 1 (PIOS Group):

Operator-blinded coronary physiology measurements will be recorded pre and post PCI.

If the post-PCI FFR is ≥0.90, no further intervention will be performed and the procedure is considered complete.

If post-PCI FFR is <0.90, the result will be disclosed to the operator and a hyperaemic pressure wire pullback during a standard peripheral intravenous adenosine infusion (140mcg/kg/min) will be performed. Depending on the result the operator would then have the following options:

A. If there is a step-up of ≥0.05 across the stented segment(s) further post-dilatation with a 0.25 - 0.50mm larger non-compliant balloon to at least 18 atmospheres should be performed followed by repeat FFR. Alternatively, the operator may choose to employ intracoronary imaging (IVUS or OCT) to guide post-dilation/optimisation of the stented segment.

B. If there is a step-up of ≥0.05 across a relatively focal (<20mm) unstented segment which is technically suitable for further stenting then a further stent should be implanted followed by repeat FFR.

C. If the FFR remains <0.90 after steps A +/- B, a further FFR pullback will be performed. If the criteria for Step B are again met, one additional stent may be deployed and a final FFR pullback performed. Following this, the FFR result will be accepted.

D. If the residual pressure gradient is interpreted to reflect diffuse atherosclerosis with no focal step-ups, the result is accepted.

E. At the end of the procedure the pressure wire sensor will be withdrawn to the tip of the guiding catheter and compared with the aortic pressure. A pressure drift of ≤0.03 will be accepted and the final FFR result adjusted accordingly.

F. If there is a drift of ≥0.04, the wire should be re-equalised and the final FFR measurement be repeated.

G. The patients will have their demographics and procedure details recorded. All patients will be asked to complete follow-up questionnaires at 3 months.

Group 2 (Control Group):

Pre and post-PCI coronary physiology measurements will be recorded but not disclosed to the operator. The angiographically defined result will be accepted. The patients will have their demographics and procedure details recorded. All patients will be asked to complete follow-up questionnaires at 3 months.

Expected value of results

1. Confirmation that the proposed PIOS protocol significantly increases the proportion of patients obtaining a physiologically optimal post-PCI result will demonstrate the feasibility of this strategy and should lead to an increase in post-PCI pressure wire usage to achieve physiologically optimal results for patients.

The investigators hypothesise that the PIOS intervention can increase the proportion of patients achieving this target from 40% to 60% and believe that an increment of at least this magnitude would be necessary to make a future larger study with both patient-oriented clinical (target vessel failure) and health care system (resource utilisation) outcomes acceptable to the interventional cardiology community and potential funders.

2. The secondary outcome measures, albeit underpowered for clinical outcomes in this study, will hopefully still give a signal that achieving a target post-PCI FFR ≥0.90 does yield objective benefits for patients. This could then form the basis for a larger phase 3 trial to confirm improved clinical outcomes and cost- effectiveness of FFR-targeted PCI

Recruitment information / eligibility

• Status: Completed
• Enrollment: 260
• Est. completion date: December 4, 2020
• Est. primary completion date: November 22, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients >18 years of age with coronary artery disease (including stable angina and stabilised non-ST-elevation myocardial infarction (NSTEMI)) who are able to provide informed consent.

Exclusion Criteria:

• PCI in a coronary artery bypass graft

• PCI to an in-stent restenosis (ISR) lesion

• PCI to a target artery providing Rentrop grade 2 or 3 collateral blood supply to another vessel

• Inability to receive adenosine (for example, severe reactive airway disease, marked hypotension, or advanced atrioventricular block without pacemaker).

• Recent (within 1 week prior to cardiac catheterization) ST-segment elevation myocardial infarction (STEMI) in any arterial distribution (not specifically target lesion).

• Severe cardiomyopathy (ejection fraction <30%).

• Renal insufficiency such that an additional 20 to 30 mL of contrast would, in the opinion of the operator, pose unwarranted risk to the patient.

Related Conditions & MeSH terms

• Coronary Artery Disease
• Coronary Stenosis

Intervention

Procedure:
• P.I.O.S.
Physiologically-Guided Incremental Optimisation Strategy

Diagnostic Test:
• Pre and post-PCI coronary physiology measurements
Pre and post-PCI coronary physiology measurements will be performed but not disclosed to the operator

Locations

Country	Name	City	State
United Kingdom	Golden Jubilee National Hospital	Glasgow

Sponsors (1)

Lead Sponsor	Collaborator
NHS National Waiting Times Centre Board

Country where clinical trial is conducted

United Kingdom, 

References & Publications (2)

Collison D, Didagelos M, Aetesam-Ur-Rahman M, Copt S, McDade R, McCartney P, Ford TJ, McClure J, Lindsay M, Shaukat A, Rocchiccioli P, Brogan R, Watkins S, McEntegart M, Good R, Robertson K, O'Boyle P, Davie A, Khan A, Hood S, Eteiba H, Berry C, Oldroyd K — View Citation

Collison D, McClure JD, Berry C, Oldroyd KG. A randomized controlled trial of a physiology-guided percutaneous coronary intervention optimization strategy: Rationale and design of the TARGET FFR study. Clin Cardiol. 2020 May;43(5):414-422. doi: 10.1002/clc.23342. Epub 2020 Feb 10. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	'As Treated' analysis of the proportion of patients with a final post-PCI FFR result =0.90	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI FFR =0.80	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change from baseline in self-reported health outcomes at 3 months as assessed by the Seattle Angina Questionnaire (SAQ)	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	3 months
Other	'As Treated' analysis of the change from baseline in self-reported health outcomes at 3 months as assessed by the EQ-5D questionnaire.	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	3 months
Other	'As Treated' analysis of the rate of target vessel failure (TVF) and its component features at 3 months.	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	3 months
Other	'As Treated' analysis of the rate of target vessel failure (TVF) and its component features at 1 year.	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 year
Other	'As Treated' analysis of the change from baseline in the FFR following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI dPR =0.90	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change from baseline in the dPR following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI RFR =0.90	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change from baseline in the RFR following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change in TTrest following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change in TThyp following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI CFR value =2.0	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change from baseline in the CFR following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI IMR >25	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the change from baseline in the IMR following PCI	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Other	'As Treated' analysis of the proportion of patients with final post-PCI IMRc >25	The primary efficacy analyses of the study intervention will be carried according to the 'intention to treat' principle (i.e. results will be compared between randomised groups according to the pre-specified outcome measures).; An 'As Treated' analysis will also be performed as an additional outcome measure. This will compare patients who actually received the PIOS intervention with those who did not.	1 day
Primary	The proportion of patients with a final post-PCI FFR result =0.90	The proportion of patients with a final post-PCI FFR result =0.90 will be compared between the randomised groups	1 day
Secondary	The proportion of patients with final post-PCI FFR =0.80	The proportion of patients with a final post-PCI FFR result =0.80 will be compared between the randomised groups	1 day
Secondary	Change from baseline in self-reported health outcomes at 3 months using a disease-specific quality of life measurement tool.	Patients will complete the Seattle Angina Questionnaire (SAQ) at baseline pre-procedure and again at 3 months post PCI	3 months
Secondary	Change from baseline in self-reported health outcomes at 3 months using a generic quality of life measurement tool.	Patients will complete the EQ-5D questionnaire at baseline pre-procedure and again at 3 months post PCI	3 months
Secondary	The rate of target vessel failure (TVF) and its component features at 3 months.	Component features of TVF include cardiac death, myocardial infarction, stent thrombosis, unplanned rehospitalisation with target vessel revascularisation.	3 months
Secondary	The rate of target vessel failure (TVF) and its component features at 1 year.	Component features of TVF include cardiac death, myocardial infarction, stent thrombosis, unplanned rehospitalisation with target vessel revascularisation.	1 year
Secondary	Change from baseline in the FFR following PCI	The difference between measurements of Fractional Flow Reserve taken in the target vessel pre- and post-PCI	1 day
Secondary	The proportion of patients with final post-PCI dPR =0.90	The proportion of patients with a final post-PCI Diastolic Pressure Ratio (dPR) value =0.90	1 day
Secondary	Change from baseline in the Diastolic Pressure Ratio (dPR) following PCI	The difference between measurements of the Diastolic Pressure Ratio taken in the target vessel pre and post PCI	1 day
Secondary	The proportion of patients with final post-PCI RFR =0.90	The proportion of patients with a final post-PCI Resting Full-cycle Ratio (RFR) value =0.90	1 day
Secondary	Change from baseline in the Resting Full-Cycle Ratio (RFR) following PCI	The difference between measurements of the Resting Full-Cycle Ratio (the lowest Pd/Pa ratio during the whole cardiac cycle at rest) taken in the target vessel pre and post PCI	1 day
Secondary	Change in TTrest following PCI	Change of the thermodilution-derived resting transit time (TTrest) from pre-PCI to final post-PCI value	1 day
Secondary	Change in TThyp following PCI	Change of the thermodilution-derived hyperaemic transit time (TThyp) from pre-PCI to final post-PCI value	1 day
Secondary	The proportion of patients with final post-PCI CFR value =2.0	The proportion of patients with a final post-PCI Coronary Flow Reserve (CFR) result =2.0	1 day
Secondary	Change from baseline in the Coronary Flow Reserve (CFR) following PCI	The difference between measurements of Coronary Flow Reserve taken in the target vessel pre and post PCI	1 day
Secondary	The proportion of patients with final post-PCI IMR >25	The proportion of patients with a final post-PCI Index of Microcirculatory Resistance (IMR) value >25	1 day
Secondary	Change from baseline in the Index of Microcirculatory Resistance (IMR) following PCI	The difference between measurements of IMR taken in the target vessel pre and post PCI	1 day
Secondary	The proportion of patients with final post-PCI IMRc >25	The proportion of patients with a final post-PCI corrected Index of Microcirculatory Resistance (IMRc) value >25	1 day
Secondary	Procedure Duration	The time required to perform the PIOS intervention procedures will be compared with those in the control group.	1 day
Secondary	The cost of additional equipment employed in the experimental arm	The cost of additional equipment employed in the PIOS intervention (i.e. balloons/stents/intra-coronary imaging).	1 day
Secondary	Fluoroscopy Dose	The radiation doses for the PIOS intervention procedures will be compared with those in the control group.	1 day
Secondary	Contrast Material Dose	The contrast material doses for the PIOS intervention procedures will be compared with those in the control group.	1 day
Secondary	Incidence of procedural complications such as coronary artery dissection or perforation.	The incidence of procedural complications such as coronary artery dissection or perforation will be recorded and compared between the two study arms	1 day