Clinical Trials Directory

Trials / Completed

CompletedNCT01485237

Severe Pandemic H1N1 Infection in ICU: Comparative Resource Utilization

Status
Completed
Phase
Study type
Observational
Enrollment
400 (actual)
Sponsor
University of Manitoba · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The main purpose of this study is to review the resource utilization of severe adult H1N1 pneumonia undergoing antiviral and oxygen therapy, mechanical ventilation and support with pulmonary rescue therapies ( nitric oxide, ECMO, HFO) in critically ill patients in Winnipeg. Secondary objectives include, comparison of resource utilization to other similar disorders (viral pneumonia, bacterial pneumonia, septic shock, ARDS). The investigators will also look at the percentage of patients that required ICU care as compared to those who could be cared for on medical wards. The investigators will determine the resources used by both groups and compare. Finally the investigators will record the frequency of chronic comorbidities in hospitalized adult H1N1 patients.

Conditions

Interventions

TypeNameDescription
OTHERWe will compare the resources used by both groupsThe main purpose of this study is to review the resource utilization. Secondary objectives include, comparison of resource utilization to other similar disorders (viral pneumonia, bacterial pneumonia, septic shock, ARDS). We will also look at the percentage of patients that required ICU care as compared to those who could be cared for on medical wards. We will determine the resources used by both groups and compare. Finally we will record the frequency of chronic comorbidities in hospitalized adult H1N1 patients.

Timeline

Start date
2009-10-01
Primary completion
2010-12-01
Completion
2012-12-01
First posted
2011-12-05
Last updated
2015-12-02

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01485237. Inclusion in this directory is not an endorsement.