Clinical Trials Directory

Trials / Completed

CompletedNCT02889770

Dead Space Monitoring With Volumetric Capnography in ARDS Patients

Dead Space Monitoring During PEEP Titration in Patients With Hypoxemia Secondary to Acute Respiratory Distress Syndrome

Status
Completed
Phase
Study type
Observational
Enrollment
10 (actual)
Sponsor
Hospital Italiano de Buenos Aires · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This studies´ objective is to describe how different PEEP levels affect dead space measured by Bohr´s formula.

Detailed description

In ARDS patients PEEP has contradictory effects on ∆P (driving pressure of the airway) hat depends on the balance between lung recruitment and overdistension. Some authors showed that incremental levels of PEEP did not much affect dead space in ARDS patients. These studies used different methods for the assessment of dead space. Such technique also overestimates the dead space. We believe that the right way to measure dead space is applying the original Bohr's equation using the mean PACO2 value. Therefore, the aim of this observational study was to describe the effect that PEEP has on Bohr's dead space and its sub-components in mechanically ventilated patients with ARDS. This observational study was performed in the Intensive Care Unit of a University Hospital. Protocol design The protocol started recording the data during baseline protective ventilation. After 15 minutes of data recording, we studied four levels of PEEP - 0, 6, 10 and 16 cmH2O - which were randomly assigned by a randomization table. Respiratory, hemodynamic, arterial blood gas analysis and volumetric capnographic parameters were recorded. We analyzed the last 2 minutes of each protocol steps consisting in more than 30 breaths or data-points.

Conditions

Interventions

TypeNameDescription
OTHERPEEP titrationExposure to different PEEP levels

Timeline

Start date
2013-09-01
Primary completion
2015-10-01
Completion
2016-06-01
First posted
2016-09-07
Last updated
2016-09-07

Source: ClinicalTrials.gov record NCT02889770. Inclusion in this directory is not an endorsement.