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.
Investigators
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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