CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 360 enrolled
Drug / intervention
Conventional circulatory support +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01633502
NCT01633502N/ACompleted

Effects of Advanced Mechanical Circulatory Support in Patients With ST Segment Elevation Myocardial Infarction Complicated by Cardiogenic Shock. The Danish Cardiogenic Shock Trial

Odense University Hospital·interventional·Posted Jul 4, 2012·Updated May 14, 2024

In Brief

A clinical study evaluating Conventional circulatory support and Impella CP for Cardiogenic Shock Acute and Acute Myocardial Infarction. Completed, enrolled 360 participants across 13 sites in 3 countries.

Detailed Summary

Cardiogenic shock a serious complication of a heart attack (myocardial infarction). Despite rapid invasive treatment, circulatory support using positive inotropes and mechanical support with intra-aortic balloon counterpulsation (IABP), and evaluation of several new treatments during the last decade, the mortality in patients with cardiogenic shock still exceeds 50%. An alternative to current management is restoration of the volume of blood pumped by the heart (cardiac output) using a ventricular assist device. In the acute setting this is difficult but can be done using the Impella device which is a catheter-based, axial flow pump that pumps blood directly from the left ventricle into the circulation thereby restoring blood flow to the failing organs. In 2012 a more powerful Impella has been introduced that is able to deliver 3.5l/min (approximately 75% of a normal cardiac output). The hypothesis of the current study is to reduce mortality and morbidity of patients with cardiogenic shock using the Impella CP. The study will be carried out as a randomized multicenter study where eligible patients will be randomized to receive conventional circulatory support or support with the Impella device and inotropic support if needed. A total of 360 patients are planned to be enrolled, and the primary endpoint will be death.

Study Details

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJul 4, 2012
Enrollment StartDec 1, 2012
Primary CompletionJul 1, 2023
Study CompletionApr 1, 2024
TodayJul 2, 2026
Enrollment to primary: 10.6 yearsPosted 14.0 years ago

Interventions

Conventional circulatory supportdevice

Control group treated with conventional circulatory support and observed in intensive care unit for a minimum of 48 hrs.

Impella CPdevice

Control group treated with Impella CP for a minimum of 48 hrs.