Interventional Left Ventricular Assist System for PCI in CHIP Patients: a Prospective, Multicenter, Noninferiority Randomized Controlled Trial

Status: Recruiting
Location: See all (15) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Mechanical circulatory support (MCS) is a life-sustaining therapy first introduced in the 1950s. After six decades of development, it now serves as a critical bridge therapy for patients with acute cardiac events and end-stage heart failure. Percutaneous mechanical circulatory support (pMCS), a key MCS modality, has advanced rapidly in recent years. In China, pMCS adoption has accelerated significantly, evidenced by year-over-year growth in both specialized centers and clinical cases, alongside continuous technological refinement. Common pMCS devices include: Intra-Aortic Balloon Pump (IABP), Axial flow pump systems (e.g., Impella®), Extracorporeal Membrane Oxygenation (ECMO). However, no randomized study has compared Impella with VA-ECMO in CHIP patients. The aim of the study is to evaluate the effectiveness and safety of interventional left ventricular assist system (VADLINK) compared to the VA-ECMO in providing circulatory support for complicated and high-risk patient with indications for PCI.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 90
Healthy Volunteers: f
View:

⁃ 1\. Aged 18-90 2. The investigator assesses that the subject requires coronary revascularization, but CABG (Coronary Artery Bypass Grafting) is considered high-risk or the subject refuses CABG. The investigator believes the subject may benefit from PCI (Percutaneous Coronary Intervention).

⁃ 3\. Left ventricular ejection fraction (LVEF) ≤ 35%. 4. Coronary angiography (CAG) or coronary computed tomography angiography (CTA) shows any of the following conditions:

• Unprotected left main (LM) coronary artery disease (coronary stenosis ≥ 50%).

• A last remaining patent coronary artery (the anterior descending artery (LAD) and/or its branches, the circumflex artery (LCX) and/or its branches, and the right coronary artery (RCA) and/or its branches).

• Saphenous vein graft (SVG) vascular lesions.

• Severely calcification, tortuosity.

• Multivessel disease (two or more) combined with chronic total occlusion (CTO).

• Three-vessel disease. Three-vessel disease is defined as significant stenosis (≥ 70%) in at least one segment of all three major epicardial coronary artery territories: the left anterior descending artery (LAD) and/or its branches, the left circumflex artery (LCX) and/or its branches, and the right coronary artery (RCA) and/or its branches. In a left-dominant coronary system, lesions in the proximal segments of the LAD and LCX are also considered three-vessel disease.

⁃ 5\. Patients who are able to give informed consent and complete the follow-up.

Locations
Other Locations
China
Beijing Tsinghua Changgung Hospital
NOT_YET_RECRUITING
Beijing
People's Hospital of Hunan Province
NOT_YET_RECRUITING
Changsha
Guangdong Provincial People's Hospital
NOT_YET_RECRUITING
Guangzhou
Nanfang Hospital Southern Medical University
NOT_YET_RECRUITING
Guangzhou
The Second Affiliated Hospital Zhejiang University School of Medicine
RECRUITING
Hangzhou
Zhejiang Hospital
NOT_YET_RECRUITING
Hangzhou
The First Hospital of Lanzhou University
NOT_YET_RECRUITING
Lanzhou
Jiangxi Provincial People's Hospital
NOT_YET_RECRUITING
Nanchang
The First Affiliated Hospital of Nanchang University
NOT_YET_RECRUITING
Nanchang
The First Affiliated Hospital of Ningbo University
NOT_YET_RECRUITING
Ningbo
The People's Hospital of Liaoning Province
NOT_YET_RECRUITING
Shenyang
Suzhou Municipal Hospital
NOT_YET_RECRUITING
Suzhou
The First Affiliated Hospital of Wenzhou Medical University
NOT_YET_RECRUITING
Wenzhou
Zhongshan Hospital Affiliated to Xiamen University
NOT_YET_RECRUITING
Xiamen
The First Affiliated Hospital of Zhengzhou University
NOT_YET_RECRUITING
Zhengzhou
Contact Information
Primary
Jun Jiang
dyjayj@qq.com
+86 135 8870 6891
Time Frame
Start Date: 2025-08-06
Estimated Completion Date: 2027-08-01
Participants
Target number of participants: 286
Treatments
Experimental: VADLINK
The VADLINK percutaneous left ventricular assist system will offer intraoperative hemodynamic support during high-risk PCI procedures.
Active_comparator: V-A ECMO
The VA-ECMO offers intraoperative hemodynamic support during high-risk PCI procedures.
Sponsors
Leads: Suzhou Hengruihongyuan Medical Technology Co. LTD

This content was sourced from clinicaltrials.gov