Skip to content

Hemodynamic and Biological Evaluations During Reventilation Collapse in ICU

Hemodynamic and Biological Evaluations During Reventilation Collapse in ICU

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01785654
Acronym
REVECOL
Enrollment
400
Registered
2013-02-07
Start date
2013-03-31
Completion date
2014-12-31
Last updated
2013-02-07

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

Conditions

Adult Patients, Arterial Line, Consent of Patients, Tracheal Intubation in ICU

Keywords

Reventilation collapse, Rate of reventilation collapse, Risk factor of reventilation collapse, Hemodynamic profile of reventilation collapse, Biologic approach of reventilation collapse

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.

Interventions

None listed

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Arterial line * Consent of patients * Adult patients * Tracheal intubation in ICU

Exclusion criteria

* tracheal intubation for cardiac arrest * pregnant woman * major protected

Design outcomes

Primary

MeasureTime frame
Reventilation collapseat day 1 (at least thirty minutes despite 500 or 1000ml of fluid resuscitation)

Secondary

MeasureTime frame
reventilation collapsein the last 72 hours
Duration of mechanical ventilationat day 1
mortalityat day 28

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferrand.fr04 73 75 11 95

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026