CLEAN ECMO: The Effects of oXiris in Cardiogenic Shock Requiring VA-ECMO

Sponsor
Samsung Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT05642273
Collaborator
(none)
60
1
2
13.2
4.6

Study Details

Study Description

Brief Summary

Cardiogenic shock (CS) defines a state of systemic hypo-perfusion leading to end-organ dysfunction related to cardiac pump failure and with mortality rates in the range of 27-50% according to recent reviews. Patients with CS often received mechanical circulatory support, and venoarterial extracorporeal membrane oxygenator (V-A ECMO) is an effective tool to support refractory CS while ensuring continuous organ perfusion. Patients with CS present clinical signs of systemic inflammation and elevated plasma levels of prototypical inflammatory and vasoactive mediators, including C-reactive protein (CRP), Interleukin-6 (IL-6) and tumor necrosis factor alpha (TNFα). As data is scarce in this field, we decided to perform a prospective randomized controlled pilot study to investigate the efficacy of extracorporeal cytokine and lipopolysaccharide adsorption using Oxiris on humoral inflammation parameters, hemodynamics, and clinical outcomes in patients with CS requiring VA ECMO.

Condition or Disease Intervention/Treatment Phase
  • Device: Oxiris membrane
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effects of extraCorporeal bLood Purification (oXiris ®) in patiEnts With cArdiogeNic Shock Requiring VA-ECMO: A Prospective, Open-label, Randomized Controlled Pilot Study
Actual Study Start Date :
Nov 25, 2022
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Oxiris for 24 h

Device: Oxiris membrane
Oxiris membrane for 24h

No Intervention: Control

Usual care

Outcome Measures

Primary Outcome Measures

  1. Change in VIS day 0 and day 2 [day 0 and day 2]

    VIS, Vasoactive Inotropic Score; dopamine dose (mg/kg/min) + dobutamine dose (mg/kg/min) + 100 x epinephrine dose (mg/kg/ min) + 10 x milrinone dose (mg/kg/min) + 10,000 x vasopressin dose (unit/kg/min) + 100 x norepinephrine dose (mg/kg/min); A high score indicates the use of a high-dose vasoactive agent.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Patients with more than 18 years old

  2. CS is defined as the presence of the following:

2-1) Systolic blood pressure is less than 90 mmHg for more than 30 minutes despite the fluid therapy, or the use of pressure boosting agents to maintain the systolic blood pressure more than 90 mmHg.

2-2) Peripheral hypoperfusion (cold skin, urine less than 30 cc per hour, impaired consciousness, lactate ≥2.0 mmol/l) or a person with pulmonary edema.

2-3) Causes of CS include ischemic (acute myocardial infarction or ischemic cardiomyopathy, shock during percutaneous coronary intervention), myocardial (end-stage heart failure, myocarditis), post-cardiotomy shock, cardiac tamponade, or pulmonary thromboembolism.

  1. Patients receiving VA ECMO owing related to the causes listed in 2-1, 2-2, 2-3.

  2. Written informed consent from patient or legal surrogates

Exclusion Criteria:
  1. Other causes except for CS: septic shock, cardiac arrest by serious ventricular arrhythmia mot related to the myocardial ischemia or heart failure.

  2. Shock with unwitnessed cardiac arrest outside the hospital

  3. Severe non-cardiac morbidity with expected survival less than 6 months (malignancy, respiratory failure)

  4. Suspicious of brain death

  5. Those who refused active treatment

  6. body weight under 30 kg

  7. Heparin allergy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Samsung Medical Center Seoul Korea, Republic of 06351

Sponsors and Collaborators

  • Samsung Medical Center

Investigators

  • Principal Investigator: Jeonghoon Yang, MD, PhD, Department of Critical Care Medicine, Samsung Medical Center, Korea

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jeong Hoon Yang, Associate professor, Samsung Medical Center
ClinicalTrials.gov Identifier:
NCT05642273
Other Study ID Numbers:
  • CLEAN ECMO
First Posted:
Dec 8, 2022
Last Update Posted:
Jan 31, 2023
Last Verified:
Jan 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 31, 2023