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PIONEER Trial:Hemodynamic Support With ECMO and IABP in Elective Complex High-risk PCI

A Prospective, Multicenter, Randomized Clinical Trial of Hemodynamic Support With ECMO and IABP Versus IABP Alone, in Complex High-risk Patients Undergoing Elective PCI(PIONEER Trial)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04045873
Enrollment
306
Registered
2019-08-06
Start date
2019-12-31
Completion date
2024-06-30
Last updated
2019-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease, Heart Failure

Keywords

Complex high-risk patients, Percutaneous coronary intervention, Extracorporeal membrane oxygenation, Intra-aortic balloon pump

Brief summary

To determine whether hemodynamic support combining VA-ECMO with IABP could mitigate the rates of Major Adverse Cardiovascular and Cerebrovascular Events (MACCEs), compared with IABP support alone, in patients undergoing elective and high-risk PCI.

Detailed description

Percutaneous Coronary Intervention (PCI) supported by mechanical circulatory device may be a viable alternative for these patients with complex coronary artery disease combined with multiple comorbidities and poor hemodynamics. Extracorporeal Membrane Oxygenation (ECMO) can direct blood flow out of the body, oxygenate it, and then return it, to either completely or partially replace the function of the heart and lungs, and potentially increase the likelihood of functional recovery. Limitations of ECMO include lack of direct LV unloading, and increased LV afterload with subsequent LV overload, which in turn can increase myocardial oxygen demand and therefore limit any cardioprotective benefits . Measures to concurrently decrease LV afterload during ECMO, such as use of an Intra-Aortic Balloon Pump (IABP), may in theory offset some of the disadvantages of ECMO. To date, ECMO has most commonly been used in patients suffering from cardiac arrest and cardiogenic shock . As far as we are aware, there exist very limited reported data from monocentric observational studies and individual case reports on the use of ECMO for elective, high-risk PCI in the literature . More importantly, no previous randomized studies to evaluate the safety and efficacy of a strategy combining VA-ECMO and IABP during high-risk PCI have been conducted to date. Most importantly, the strategy of combined VA-ECMO and IABP has never been investigated in any randomized trial that we could find.

Interventions

DEVICEextracorporeal membrane oxygenation

The VA-ECMO procedure will be performed by femoral artery access, and the IABP will then be implanted in the contralateral femoral artery.

Sponsors

The First Affiliated Hospital of Zhengzhou University
CollaboratorOTHER
Bethune International Peace Hospital
CollaboratorOTHER
Beijing Anzhen Hospital
CollaboratorOTHER
The Second Affiliated Hospital of Harbin Medical University
CollaboratorOTHER
The General Hospital of Northern Theater Command
CollaboratorOTHER
Xijing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Patients aged from 18 years to 85 years who meet any one of the following criteria 1. Unprotected left main coronary artery disease with severe LV dysfunction (EF\<35% or NYHA grade Ⅲ and Ⅳ). 2. Unprotected left main coronary artery disease without severe LV dysfunction (LVEF\>35% or NYHA Ⅰ and Ⅱ) must meet at least two of the complex procedure criteria (see Section II below). 3. 3-vessel disease with severe LV dysfunction (EF\<35% or NYHA grade Ⅲ and Ⅳ) must meet at least two of the complex procedure criteria (see Section II below). Criteria Defining a Complex Procedure 1. Bifurcation requiring PCI in two branches (including PTCA or stenting). 2. Calcification requiring atherectomy. 3. Tortuosity requiring device assistance. 4. Difficult CTO(J-CTO score≥2).

Exclusion criteria

1. Acute myocardial infarction within the previous 48 hours. 2. Pre-procedure cardiac arrest within 24 hours of enrollment requiring CPR. 3. Cardiogenic shock. 4. Complications of acute myocardial infarction (including ventricular septal defect, severe mitral regurgitation, and intractable ventricular arrhythmias). 5. Contraindications to IABP or ECMO use, including significant iliac or femoral arterial disease and more than mild aortic regurgitation as seen on echocardiography. 6. Bleeding diathesis or warfarin therapy with an international normalized ratio greater than 2.5. 7. Active internal bleeding (including menstruation) within the past month. 8. Recent ischemic stroke within the past month diagnosed by CT or MRI. 9. Previous hemorrhagic stroke diagnosed by CT or MRI. 10. Allergy to aspirin, clopidogrel, heparin, ticagrelor or glycoprotein IIb/ IIIa inhibitors; thrombocytopenia. 11. Pregnancy. 12. Current enrollment in any other study.

Design outcomes

Primary

MeasureTime frameDescription
The primary efficacy end point is the composite rate of MACCE at peri-procedure, in-hospital, or within a 30-day follow-up post-discharge.30 daysThe composite primary end point components include angiographic failure rates of PCI, all-cause death, myocardial infarction, stroke or transient ischemic attack, any repeat revascularization procedure, acute renal insufficiency, major vascular complications, severe intraprocedural hypotension requiring therapy, cardiopulmonary resuscitation, or ventricular tachycardia requiring cardioversion.

Secondary

MeasureTime frame
intra-procedure hemodynamicsintra-procedure
vascular access site and access-related complicationsintra-procedure
major or life-threatening or disabling bleeding30 days
stroke or transient ischemic attack30 days
The rate of complete revascularizationintra-procedure
MACCE at 6 months6 months
MACCE at 1 year1 year
MACCE at 2 years2 years
MACCE at 3 years3 years
acute kidney injury30 days

Contacts

Primary ContactYi Liu, MD, PhD
liuyimeishan@hotmail.com86-02984775183

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026