Actively Recruiting

Age: 18Years +
All Genders
NCT07402018

Intra-aortic Balloon Counterpulsation (IABC) Compliance

Led by Thomas Jefferson University · Updated on 2026-02-11

20

Participants Needed

1

Research Sites

48 weeks

Total Duration

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AI-Summary

What this Trial Is About

The investigators intend to study how baseline arterial compliance (as defined by stroke volume/pulse pressure) influences the clinical success of intraaortic balloon counterpulsation (IABC) in patients with cardiogenic shock (CS). The investigators aim to compare clinical outcomes in CS patients requiring IABC with normal compliance versus low compliance. The study will enroll patients undergoing IABC that are clinically indicated. Baseline hemodynamic measurements will be obtained and then patients would be stratified based on their compliance. Post IABC, serial hemodynamic measurements will be obtained and compared between groups. Patients will continue to be followed longitudinally until the IABC has been discontinued for any reason. The proposed study will yield results that will aid in developing a larger clinical trial and ultimately assist clinicians in determining if IABC is appropriate therapy for patients in cardiogenic shock.

CONDITIONS

Official Title

Intra-aortic Balloon Counterpulsation (IABC) Compliance

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with cardiogenic shock
  • Undergoing intra-aortic balloon counterpulsation (IABC) as part of clinical care
  • Able to provide consent or have power of attorney or next of kin provide consent
Not Eligible

You will not qualify if you...

  • Under 18 years old
  • Unable to provide consent and no power of attorney or next of kin to consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

Thomas Jefferson University Hospital

Philadelphia, Pennsylvania, United States, 19107

Actively Recruiting

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Research Team

E

Elizabeth R Westburg, MS

CONTACT

M

Matthew S Delfiner, DO, MS

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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