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Clinical Trials/NCT02866513
NCT02866513
Completed
N/A

Incidence of High Levels of Transpulmonary Pressure During the Use of Airway Pressure Release Ventilation.

Assistance Publique Hopitaux De Marseille1 site in 1 country20 target enrollmentFebruary 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Patient Mechanically Ventilated With APRV Mode
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
20
Locations
1
Primary Endpoint
Transpulmonary pressure
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Mechanical ventilation can induce pulmonary lesions called ventilator induced lung injury (VILI). High levels of Transpulmonary pressure is one of the most important mechanism of VILI during the use of mechanical ventilation. The use of bilevel pressure ventilator modes like APRV could generate high levels of transpulmonary pressure.

The aim of this study is to evaluate the variations of transpulmonary pressure during the use of APRV by clinicians

Registry
clinicaltrials.gov
Start Date
February 2016
End Date
March 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient mechanically ventilated for more than 48 H for acute respiratory failure
  • Decision to use of the APRV mode by clinicians in charge of the patient

Exclusion Criteria

  • Contraindication for the use of a nasogastric tube

Outcomes

Primary Outcomes

Transpulmonary pressure

Time Frame: 24 hours

Measurement of transpulmonary pressure needs the measurement of oesophageal pressure with a specific nasogastric tube. This measurement is now available in routine in few mechanical ventilators in intensive care units (eg: AVEA Ventilator. Vyasys HealthCare). Transpulmonary pressure is the difference between airway pressure and oesophageal pressure and it is now easy to obtain and monitor at the bedside with these ventilators. It is also possible to record the value furthermore than 24 hours.

Secondary Outcomes

  • Maximal value of transpulmonary pressure(24 hours)

Study Sites (1)

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