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NCT07402018 · ClinicalTrials.gov registry record
Intra-aortic Balloon Counterpulsation (IABC) Compliance
A clinical trial of Cardiogenic Shock and IABC Procedure, sponsored by Thomas Jefferson University.
- Recruiting
- Registry status
- 20
- Enrollment target
- 1
- Study location
NCT07402018 is a study of Cardiogenic Shock and IABC Procedure that is actively recruiting participants, run by Thomas Jefferson University. The registered enrollment target is 20 participants, below the 633-participant average among 16 other Cardiogenic Shock trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.
The verdict
NCT07402018, a study of Cardiogenic Shock and IABC Procedure, is actively recruiting participants, sponsored by Thomas Jefferson University.
- RECRUITING
- Registry status
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
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 Studied
Study Locations (1)
Pennsylvania
- Thomas Jefferson University Hospital - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2026-01-27 |
| Est. Completion | 2026-12-31 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07402018
The ClinicalTrials.gov registry entry for NCT07402018 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 633-participant average among 16 other Cardiogenic Shock trials with a reported enrollment target (97% lower). The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Cardiogenic Shock appearing as the primary indexed condition, and to 0 interventions.
NCT07402018 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07402018 about?
NCT07402018 is a clinical study titled "Intra-aortic Balloon Counterpulsation (IABC) Compliance". 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 re...
What is the current status of trial NCT07402018?
This trial is currently recruiting. The enrollment target is 20 participants. The study started on 2026-01-27. Estimated completion is 2026-12-31.
What conditions does trial NCT07402018 study?
This clinical trial studies the following conditions: Cardiogenic Shock, IABC Procedure, Intraaortic Balloon Counterpulsation (IABC).
Who is sponsoring clinical trial NCT07402018?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07402018 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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