Usefulness of the Use of Co-registration Strategy With iFR in Long and/or Diffuse Coronary Lesions

NCT ID: NCT04283734

Last Updated: 2023-10-02

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-02-11
• Study Completion Date: 2024-01-24

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 the potencial benefit in terms of MACEs reduction at follow-up with respect to angiographic guiding of percutaneous coronary intervention (control group).

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 analysis of the physiological importance of every lesion and every coronary segment. This fact has allowed to create a new specific software. Syncvision show us the functional compromise of every lesion and predict the expected IFR improvement.

This potential benefit could have an extra benefit in the reduction of the implanted stent length. There are some observational study published that reported a reduction of 5 mm of stent length, but we think that the reduction could be significantly higher.

However, this reduction could be detrimental of the complete cover of plaque in this type of lesion, which has also proved to be a predictor of MACEs.

For this reason, we have proposed to perform a randomized study to define if the utilization of physiological IFR pullback evaluation in long and/or diffuse coronary lesion present advantages over classical angiographic PCI.

Study hyphotesis:

Revascularization guided by IFR-Pullback in long and/or diffuse coronary lesions permit to reduce the stent length implanted, with the potential benefit in terms of MACEs reduction.

Study design:

Randomized and controlled study where we will include patients with significant coronary stenosis at least in one vessel and a total lesion length higher than 30 mm in the different clinical scenarios (stable angina, NSTEMI and STEMI in non-culprit lesion).

In the control group, stent length will be decided by the operator. In the iFR-pullback group, stent length will be decided in base to iFR expected, trying to obtain an IFR of 0.90 with the minimum stent length as possible.

The expected stent length reduction is 15 mm (primary endpoint). As secondary endpoint, we will analyze the combined endpoint of myocardial infarction, death and new revascularization).

The sample size in base to primary endpoint will be of 100 patients.

Conditions

Instantaneous Wave Free Ratio; Diffuse Coronary Artery Disease; Long Coronary Lesion; Syncvision Software

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Intervention group

Long/diffuse coronary lesion should be evaluated and guided by iFR pullback with Syncvision software to achieve a final iFR of 0.90

Group Type: EXPERIMENTAL

iFR pullback with Syncvision software (Volcano company)

Intervention Type: DEVICE

iFR pullback with Syncvision software permit us to analyze the vessel completely and to predict the physiological significance of every lesion and segment, to predict the benefit of the revascularization in terms of iFR improvement, and to predict the minimum stent length necessary to achieve this improvement.

Control group

Long/diffuse coronary lesion should be treated guided by angiography

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

iFR pullback with Syncvision software (Volcano company)

iFR pullback with Syncvision software permit us to analyze the vessel completely and to predict the physiological significance of every lesion and segment, to predict the benefit of the revascularization in terms of iFR improvement, and to predict the minimum stent length necessary to achieve this improvement.

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

• 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 Criteria

• 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.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Maimónides Biomedical Research Institute of Córdoba

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Francisco Hidalgo, PhD

Role: PRINCIPAL_INVESTIGATOR

Hospital Universitario Reina Sofía

Locations

Hospital Universitario Reina Sofía

Córdoba, , Spain

Countries

Spain

References

Hidalgo F, Gonzalez-Manzanares R, Suarez de Lezo J, Gallo I, Alvarado M, Perea J, Maestre-Luque LC, Resua A, Romero M, Lopez-Benito M, Perez de Prado A, Ojeda S, Pan M. The Usefulness of Coregistration with iFR in Tandem or Long Diffuse Coronary Lesions: The iLARDI Randomized Clinical Trial. J Clin Med. 2024 Jul 25;13(15):4342. doi: 10.3390/jcm13154342.

Reference Type: DERIVED

PMID: 39124613 (View on PubMed)

Other Identifiers

iLARDI

Identifier Type: -

Identifier Source: org_study_id