Hemodynamic and Biological Evaluations During Reventilation Collapse in ICU
- Conditions
- Consent of PatientsAdult PatientsArterial LineTracheal Intubation in ICU
- Registration Number
- NCT01785654
- Lead Sponsor
- University Hospital, Clermont-Ferrand
- Brief Summary
Prospective, observational clinical multicentric study in ICU; during the period surrounding the orotracheal intubation.
- Detailed Description
Main objective: to describe the characteristics of reventilation collapse: collapse rate, duration and treatment implemented
Secondary objectives:
* identify risk factors of reventilation collapse
* compare mortality, hemodynamic, respiratory, infectious and biological data between collapse group and no reventilation collapse group.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria
- Arterial line
- Consent of patients
- Adult patients
- Tracheal intubation in ICU
Exclusion Criteria
- tracheal intubation for cardiac arrest
- pregnant woman
- major protected
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reventilation collapse at day 1 (at least thirty minutes despite 500 or 1000ml of fluid resuscitation)
- Secondary Outcome Measures
Name Time Method mortality at day 28 reventilation collapse in the last 72 hours Duration of mechanical ventilation at day 1
Trial Locations
- Locations (1)
CHU Clermont-Ferrand
🇫🇷Clermont-Ferrand, France