Distal Evaluation of Functional Performance With Intravascular Sensors to Assess the Narrowing Effect: Guided Physiologic Stenting (DEFINE GPS)

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Philips

Status

Invitation-only

Conditions

Ischemic Heart Disease
Coronary Artery Disease

Treatments

Device: Philips SyncVision system with Philips pressure wires
Procedure: standard of care angiographically-guided PCI

Study type

Interventional

Funder types

Industry

Identifiers

NCT04451044
190103

Details and patient eligibility

About

Multi-center, prospective, randomized controlled study comparing PCI guided by angiography versus iFR Co-Registration using commercially available Philips pressure guidewires and the SyncVision co-registration system, employing an adaptive design study for interim sample size re-estimation.

Enrollment

3,212 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

* 1. Adult men and women (local age of consent) who present with stable or unstable angina, or NSTEMI. * 2. Undergoing cardiac catheterization with planned PCI or possible ad hoc PCI * 3. Following angiography, PCI is indicated in at least one coronary artery\* on the basis of one or more of the following: 1. Presenting with NSTE-ACS (unstable angina with ECG changes or cardiac enzyme-positive NSTEMI) with an identified culprit lesion with DS ≥50%; 2. One or more angiographic stenoses present with ≥80% stenosis severity by visual estimation; 3. One or more angiographic stenoses present with ≥50% to \<80% stenosis severity by visual estimation and an abnormal non-invasive stress test in the distribution of the lesion(s) within the past 60 days; 4. One or more angiographic stenoses are present with ≥50% to \<80% stenosis severity by visual estimation and a spot iFR measure ≤0.89 or FFR≤0.80 for borderline iFR.. * 4 Subject is willing to comply with all scheduled visits and tests and has provided informed written consent

Exclusion criteria

* 1. STEMI within 30 days * 2. PCI within the prior 12 months, or any PCI planned after the study procedure (other than planned staged procedures of randomized vessels which are allowed) * 3. Prior CABG anytime * 4. Silent ischemia only (i.e. no cardiac symptoms related to coronary artery disease) within the prior 4 weeks * 5. Documented prior iFR pullback performed in any coronary artery including during the qualifying diagnostic angiogram * 6. Any vessel with in-stent restenosis (ISR) requiring treatment * 7. Cardiogenic shock defined as systolic blood pressure \<90 mmHg for \>20 minutes not responding to fluid resuscitation, or need for inotropic, pressor, or device-based hemodynamic support * 8. Presence of unstable ventricular arrhythmias * 9. Heart rate \> 110, including uncontrolled atrial fibrillation (AF) * 10. Decompensated congestive heart failure (NYHA Class IV or Killip Class III or IV) * 11. Chronic total occlusion (CTO) of a target vessel (exception: a CTO may be present in a non-target vessel if it is supplying non-viable myocardium and there is no intent to open the CTO during the index or later procedure) * 12. Coronary anatomy not amenable to pressure wire manipulation due to extreme tortuosity or complexity such that it is unlikely that a pressure wire could be passed to the distal third of the three major epicardial coronary arteries * 13. Any angiographic giant thrombus (i.e., thrombus length \> 3x RVD at lesion) * 14. Any target vessel with \< TIMI III flow * 15. Any target lesion with a reference vessel diameter (RVD) less than 2.25mm except for within the side branch of a bifurcation lesion * 16. Any non-target lesion with a reference vessel diameter (RVD) greater than 2.00mm that contains an ≥80% stenosis and is not intended for treatment with PCI (other than a CTO supplying non-viable myocardium - see exclusion #11) * 17. Known severe aortic or mitral valve stenosis/insufficiency * 18. Known non-cardiovascular comorbidity resulting in lifespan \<24 months * 19. Known left ventricular ejection fraction ≤30% * 20. Estimated creatinine clearance (MDRD formula) \<30 mL/min/1.73m2 or on dialysis * 21. Any cardiac or non-cardiac surgical procedure planned within 12 months after enrollment, or any procedure planned within 6 months after enrollment that would necessitate discontinuation of dual antiplatelet therapy * 22. Known pregnancy or planning to become pregnant (women of child-bearing potential must have a negative pregnancy test within 1 week of enrollment) * 23. Participating in another investigational drug or device study that has not reached its primary endpoint * 24. Any condition such as dementia or substance abuse that may impair the patient's ability to comply with all study procedures, including medication compliance and follow-up visits * 25. Patient is a member of a vulnerable population who, in the judgment of the investigator, is unable to give Informed Consent for reasons of incapacity, immaturity, adverse personal circumstances or lack of autonomy. This may include individuals with mental disability, persons in nursing homes, children, impoverished persons, persons in emergency situations, homeless persons, nomads, refugees, and those permanently incapable of giving informed consent. Vulnerable populations also include university students, subordinate hospital and laboratory personnel, employees of the Sponsor, members of the armed forces, and persons kept in detention.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

3,212 participants in 2 patient groups

physiologically-guided arm
Experimental group
Description:
Physiologically-guided PCI using the Philips SyncVision system for determining the PCI strategy
Treatment:
Device: Philips SyncVision system with Philips pressure wires
angiographically-guided arm
Active Comparator group
Description:
Standard of care angiographically-guided PCI for determining the PCI strategy
Treatment:
Procedure: standard of care angiographically-guided PCI

Trial contacts and locations

72

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Data sourced from clinicaltrials.gov

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