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Effets hémodynamiques de l’administration de vasopressine au décours de l’Arrêt Cardio-Respiratoire chez des patients en état de choc réfractaireHemodynamic effects of vasopressin administration in patient with refractory shock following successfully resuscitated cardiac arrest

Active, not recruiting
Conditions
Patients admitted in ICU after sucessfully resuscitated cardiac arrest and developping a refractory shock
MedDRA version: 8.1Level: LLTClassification code 10047146Term: Vasopressin
Registration Number
EUCTR2006-005421-31-FR
Lead Sponsor
RER Saint Denis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
10
Inclusion Criteria

Patient admitted after successfully resuscitated cardiac arrest requiring high level of vasopressor support
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Age <18
Cardiac index < 2.5 l/min/square meter
or Svo2 < 70%

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: A decrease of the need of vasopressor support.;Secondary Objective: Evolution of venous oxygen saturation and organ dysfunction score (LOD, SOFA);Primary end point(s): Decrease in the need of vasopressor support
Secondary Outcome Measures
NameTimeMethod
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