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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 réfractaire Hemodynamic effects of vasopressin administration in patient with refractory shock following successfully resuscitated cardiac arrest

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

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-005421-31-FR
Enrollment
10
Registered
2007-03-06
Start date
2007-04-24
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients admitted in ICU after sucessfully resuscitated cardiac arrest and developping a refractory shock MedDRA version: 8.1 Level: LLT Classification code 10047146 Term: Vasopressin

Interventions

Trade Name: PITRESSIN Product Name: Arginine Vasopressine (Pitressin) Pharmaceutical Form: Intravenous infusion Other descriptive name: VASOPRESSIN Concentration unit: IU international unit(s) Concent

Sponsors

RER Saint Denis
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

Countries

France

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026