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Mechanical Circulatory Support Device

Impella-CP LV Vent for Cardiogenic Shock (REVERSE Trial)

N/A
Waitlist Available
Led By Christian Bermudez, MD
Research Sponsored by University of Pennsylvania
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up at discharge from hospital, an average of 60 days
Awards & highlights

REVERSE Trial Summary

This trial is testing whether adding a left ventricular assist device (Impella CP) to veno-arterial extracorporeal membrane oxygenation (VA-ECMO) improves survival and cardiac recovery in cardiogenic shock patients.

Eligible Conditions
  • Cardiogenic Shock

REVERSE Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at thirty days.
This trial's timeline: 3 weeks for screening, Varies for treatment, and at thirty days. for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Recovery from cardiogenic shock.
Secondary outcome measures
Survival to hospital discharge.

REVERSE Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: ExperimentalExperimental Treatment1 Intervention
VA-ECMO with early institution of Impella CP LV venting
Group II: ControlActive Control1 Intervention
VA-ECMO alone per standard clinical protocol.

Find a Location

Who is running the clinical trial?

University of PennsylvaniaLead Sponsor
2,005 Previous Clinical Trials
42,882,194 Total Patients Enrolled
Christian Bermudez, MDPrincipal InvestigatorUniversity of Pennsylvania
Michael Ibrahim, MD PhDPrincipal Investigator - University of Pennsylvania
Hackensack University Medical Center, Holy Name Hospital, Hackensack University Medical Center at Pascack Valley
Medical School - University of Alexandria Faculty of Medicine, Bachelor of Medicine, Bachelor of Surgery
Nassau University Medical Center, Residency in Internal Medicine

Media Library

Impella-CP LV Vent (Mechanical Circulatory Support Device) Clinical Trial Eligibility Overview. Trial Name: NCT03431467 — N/A
Cardiogenic Shock Research Study Groups: Control, Experimental
Cardiogenic Shock Clinical Trial 2023: Impella-CP LV Vent Highlights & Side Effects. Trial Name: NCT03431467 — N/A
Impella-CP LV Vent (Mechanical Circulatory Support Device) 2023 Treatment Timeline for Medical Study. Trial Name: NCT03431467 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Does this inquiry accommodate individuals aged 65 and above?

"This medical trial seeks individuals aged 18 to 65, with 13 studies available for patients under the legal age of consent and 132 trials targeting those beyond retirement age."

Answered by AI

Is there still an opportunity for individuals to join this clinical research?

"This specific medical trial, which was initially posted on March 19th of 2018 and last updated November 4th 2022, is no longer recruiting. However, clinicaltrials.gov currently lists over a hundred and forty two other studies actively seeking participants."

Answered by AI

Who is eligible to participate in this scientific research?

"This clinical trial seeks to include 96 individuals aged 18-65 suffering from cardiogenic shock due to Post-acute myocardial infarction, drug overdose, early graft failure post orthotropic heart transplantation or acute on chronic cardiomyopathy with progressive shock and decompensation. Candidates must have no mechanical complications requiring surgical intervention after extracorpeal membrane oxygenator (ECMO) such as post-ischaemic ventricular septal defect (VSD)."

Answered by AI
~2 spots leftby Apr 2025