Clinical Trials Directory

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UnknownNCT01366274

Protective Manual Hyperinflation in Acute Mechanically Ventilated Trauma Patients

Comparison of Protective Manual Hyperinflation With Current Methods in Ventilated Acute Trauma Patients: a Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
The University of Queensland · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This single-blinded randomized study aims to compare two methods of manual hyperinflation (protective - moderate tidal volumes with positive end expiratory pressure) and non-protective (large tidal volume and no positive end expiratory pressure) in ventilated acute trauma patients, to investigate the effect on inflammatory markers, lung compliance, oxygenation and sputum volume.

Detailed description

Current evidence in mechanical ventilation supports a "protective lung strategy" that is, smaller tidal volumes and prevention of loss of positive end expiratory pressure (PEEP). There is concern that manual hyperinflation (MHI) may conflict with this strategy and cause volutrauma and atelectrauma potentially leading to biotrauma. This single-blinded randomized study aims to compare two methods of manual hyperinflation (protective - moderate tidal volumes with positive end expiratory pressure) and non-protective (large tidal volume and no positive end expiratory pressure) in ventilated acute trauma patients, to investigate the effect on inflammatory markers, lung compliance, oxygenation and sputum volume.

Conditions

Interventions

TypeNameDescription
OTHERProtective manual hyperinflationManual hyperinflation for 10 minutes using a Mapleson C circuit and 100% oxygen with volume set at 8mls/kg and positive end expiratory pressure in the circuit appropriate to baseline levels
OTHERUsual method of MHIManual hyperinflation for 10 minutes using a Mapleson C circuit and 100% oxygen with volume set at 12mls/kg and no positive end expiratory pressure in the circuit

Timeline

Start date
2007-09-01
Primary completion
2011-12-01
Completion
2011-12-01
First posted
2011-06-06
Last updated
2011-06-06

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT01366274. Inclusion in this directory is not an endorsement.