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Clinical Trials/DRKS00025265
DRKS00025265
Recruiting
未知

Impact of a VA-ECMO in combination with an extracorporeal cytokine hemadsorption system in critically ill patients with cardiogenic shock.A prospective, randomized, controlled, blinded, monocenter, trial - ECMOsorb

niversitätsklinikum Jena KIM I, Kardiologie0 sites54 target enrollmentMay 12, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
R57.0
Sponsor
niversitätsklinikum Jena KIM I, Kardiologie
Enrollment
54
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 12, 2021
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Sponsor
niversitätsklinikum Jena KIM I, Kardiologie

Eligibility Criteria

Inclusion Criteria

  • Critically ill patients with cardiogenic shock with or without reanimation (CPR),
  • \- indication for VA\-ECMO,
  • \- age \=18 years \=80 years.
  • \- signed informed consent

Exclusion Criteria

  • Contraindications to VA\-ECMO implantation.
  • Patients with pre – existing sepsis (raised CRP, positive PCT, leukocytosis, fever, positive blood cultures).
  • Shock duration\> 12 h before evaluation.
  • Severe PVD (peripheral vessel disease) making ECMO\-implantation impossible.
  • Aortic valve insufficiency / stenosis at least II °.
  • Age \<18, \> 80 years.
  • CNS disease with fixed, dilated pupils (not drug\-induced).
  • Severe concomitant disease with limited life expectancy \<6 months.
  • Participation in another study.
  • CPR\> 60min.

Outcomes

Primary Outcomes

Not specified

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