Cardiogenic Shock Clinical Trial
— EARLY-UNLOADOfficial title:
Early Left Atrial Septostomy Versus Conventional Approach After Venoarterial Extracorporeal Membrane Oxygenation: A Randomized Controlled Study
Verified date | January 2024 |
Source | Chonnam National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The use of venoarterial-extracorporeal membrane oxygenation(VA-ECMO) was associated with lower in-hospital mortality in patients with cardiogenic shock. However, VA-ECMO has a deleterious effect for hemodynamics. It can increase left ventricular end-diastolic pressure(LVEDP), followed by left ventricular dilatation, abnormal opening of aortic valve and jeopardizes of myocardial recovery. Therefore, several methods have been used to reduce LVEDP. Among these, left atrial septostomy is effective, but less invasive than surgical left ventricular unloading. However, there is few data regarding this issue. Therefore, the investigators will evaluate the effect of routine, early left atrial septostomy in patients with VA-ECMO for the treatment of cardiogenic shock.
Status | Completed |
Enrollment | 116 |
Est. completion date | October 31, 2023 |
Est. primary completion date | March 14, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: 1) Age more than 18 years old 2) Cardiogenic shock* 3) Successful VA-ECMO implantation - The definition of cardiogenic shock All these criteria should be met 1. Systolic blood pressure < 90 mmHg for 30 minutes, or needing inotrope or vasopressor to maintain systolic blood pressure > or = 90 mmHg 2. Pulmonary congestion on chest X-ray or increased left ventricular filling pressure by cardiac catheterization 3. At least one criteria of organ dysfunction - mental obtundation, clammy skin, oliguria, renal dysfunction, increased level of blood lactate Exclusion Criteria: 1. VA-ECMO after open heart surgery 2. VA-ECMO for the treatment of non-cardiac shock 3. Severe bleeding* 4. Terminal malignancy 5. Irreversible brain damage 6. Pregnancy or lactation - The definition of severe bleeding Hemoglobin decrease after VA-ECMO or cannulation site bleeding is not a exclusion criteria 1. Hypovolemic shock due to definite bleeding cause 2. Identifiable bleeding causes: gastrointestinal bleeding, hemothorax, traumatic bleeding, central nervous system hemorrhage, pulmonary hemorrhage |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Chonnam National University Hospital | Gwangju |
Lead Sponsor | Collaborator |
---|---|
Chonnam National University Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cumulative incidence rate of all-cause death | Cumulative incidence rate of all-cause death | Up to 30 days | |
Secondary | Rate of all-cause death or left atrial septostomy in conventional approach group | Rate of all-cause death or left atrial septostomy in conventional approach group | Up to 30 days | |
Secondary | Rate of left atrial septostomy in conventional approach group | Rate of left atrial septostomy in conventional approach group | Up to 30 days | |
Secondary | Incidence rate of all-cause death during index admission | Incidence rate of all-cause death during index admission | Up to 6 months | |
Secondary | Cumulative incidence rate of cardiac death | Cumulative incidence rate of cardiac death | Up to 30 days | |
Secondary | Cumulative incidence rate of non-cardiac death | Cumulative incidence rate of non-cardiac death | Up to 30 days | |
Secondary | Weaning rate from venoarterial extracorporeal membrane oxygenation during index admission | Weaning rate from venoarterial extracorporeal membrane oxygenation during index admission | Up to 6 months | |
Secondary | Rate of disappearance of pulmonary edema on chest X-ray during index admission | Rate of disappearance of pulmonary edema on chest X-ray during index admission | Up to 6 months | |
Secondary | Weaning rate from mechanical ventilator during index admission | Weaning rate from mechanical ventilator during index admission | Up to 6 months | |
Secondary | Intensive care unit length of stay during index admission | Intensive care unit length of stay during index admission | Up to 6 months | |
Secondary | Hospital length of stay | Hospital length of stay | Up to 6 months | |
Secondary | Lactate normalization rate | Lactate normalization rate | Up to 30 days | |
Secondary | Lactate clearance rate | Lactate clearance rate | Up to 30 days | |
Secondary | Rate of renal replacement therapy during index admission | Rate of renal replacement therapy during index admission | Up to 6 months | |
Secondary | Rate of limb ischemia during index admission | Rate of limb ischemia during index admission | Up to 6 months | |
Secondary | Rate of infection during index admission | Rate of infection during index admission | Up to 6 months | |
Secondary | Rate of transient ischemic attack or stroke during index admission | Rate of transient ischemic attack or stroke during index admission | Up to 6 months | |
Secondary | Rate of BARC bleeding type 3 or 5 during index admission | Rate of BARC bleeding type 3 or 5 during index admission | Up to 6 months | |
Secondary | Rate of bridge to ventricular assist device or heart transplantation during index admission | Rate of bridge to ventricular assist device or heart transplantation during index admission | Up to 6 months | |
Secondary | Rate of major vascular injury or cardiac tamponade during left atrial septostomy | Rate of major vascular injury or cardiac tamponade during left atrial septostomy | Up to 30 days | |
Secondary | Cumulative incidence rate of all-cause death | Cumulative incidence rate of all-cause death | Up to 12 months | |
Secondary | Cumulative incidence rate of cardiac death | Cumulative incidence rate of cardiac death | Up to 12 months | |
Secondary | Cumulative incidence rate of non-cardiac death | Cumulative incidence rate of non-cardiac death | Up to 12 months | |
Secondary | Re-hospitalization rate due to heart failure | Re-hospitalization rate due to heart failure | Up to 12 months | |
Secondary | All-cause death or re-hospitalization rate due to heart failure | All-cause death or re-hospitalization rate due to heart failure | Up to 12 months |
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT03283995 -
Hemodynamic Assessment in Cardiogenic Shock Regarding the Etiology
|
||
Active, not recruiting |
NCT04325035 -
The Safety and Efficacy of Istaroxime for Pre-Cardiogenic Shock
|
Phase 2 | |
Active, not recruiting |
NCT05100836 -
SURPASS Impella 5.5 Study
|
||
Not yet recruiting |
NCT05106491 -
Efficacy and Safety of Synchronized Cardiac Support in Cardiogenic Shock Patients
|
N/A | |
Completed |
NCT02301819 -
ExtraCorporeal Membrane Oxygenation in the Therapy of Cardiogenic Shock
|
N/A | |
Completed |
NCT01367743 -
Study Comparing the Efficacy and Tolerability of Epinephrine and Norepinephrine in Cardiogenic Shock
|
Phase 4 | |
Recruiting |
NCT05728359 -
Genomic Determinants of Outcome in Cardiogenic Shock
|
||
Recruiting |
NCT05699005 -
Individualized or Conventional Transfusion Strategies During Peripheral VA-ECMO
|
Phase 1 | |
Not yet recruiting |
NCT06338345 -
Pharmacokinetics and Modelling of Beta-Lactam in ECMO-VA Patients
|
N/A | |
Completed |
NCT03436641 -
Microcirculation in Cardiogenic Shock
|
||
Recruiting |
NCT03313687 -
SafeTy and Outcome of contemPorary Treatment Strategies for Cardiogenic SHOCK
|
||
Recruiting |
NCT05506449 -
The RECOVER IV Trial
|
N/A | |
Completed |
NCT04144660 -
"Treatment Use of ECMO In Pregnancy or Peripartum Patient."
|
||
Completed |
NCT04548739 -
Cerebral Autoregulation in Pediatric ECMO (ECMOX 2)
|
||
Recruiting |
NCT04141410 -
Global Longitudinal Strain Assessment in Cardiogenic Shock During Sepsis
|
||
Not yet recruiting |
NCT05879276 -
Effect at 3 Months of Early Empagliflozin Initiation in Cardiogenic Shock Patients on Mortality, Rehospitalization, Left Ventricular Ejection Fraction and Renal Function.
|
Phase 3 | |
Enrolling by invitation |
NCT05570864 -
Score TO Predict SHOCK - STOP SHOCK
|
||
Completed |
NCT02591771 -
Study of Multistep Pharmacological and Invasive Management for Cardiogenic Shock
|
Phase 2 | |
Terminated |
NCT02279979 -
Thoratec Corporation HeartMate PHP™ Cardiogenic Shock Trial
|
N/A | |
Completed |
NCT01374867 -
CardShock Study and Registry
|
N/A |