Clin2
NCT07149714Possibly a fitRecruiting

Heart pump support for high-risk angioplasty

Ischemic Cardiovascular DiseaseMultivessel Coronary Artery DiseaseCoronary Artery DiseaseCardiogenic ShockAcute Heart Failure (AHF)Chronic Heart FailurePercutaneous Coronary Intervention

Part of Heart & circulation clinical trials.

This trial tests the iVAC 2L device, a temporary heart pump placed in the main artery, to help patients who need a high-risk angioplasty (PCI) because of a very narrowed or blocked coronary artery. The goal is to prevent the heart from failing during the procedure.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
100 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Your heart team has decided that your angioplasty has a high risk of causing your heart to collapse.
  • You have signed a consent form to participate in the study.
  • The artery in your groin (femoral artery) must be at least 6 millimeters wide.
  • You cannot have heart failure involving both sides of the heart or mainly the right side.
  • You must not have a blood clot in the left lower heart chamber, a mechanical heart valve, or severe aortic valve disease.
  • You cannot have severe peripheral artery disease that would block the placement of the pump.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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