Pneumonia, Ventilator Associated Clinical Trial
Official title:
Endotracheal Suction With or Without Daily Changes of Closed System Suction. Effect on Ventilator Associated Pneumonia and Cost
Verified date | March 2007 |
Source | Bayside Health |
Contact | n/a |
Is FDA regulated | No |
Health authority | Australia: National Health and Medical Research Council |
Study type | Interventional |
The purpose of this study was to compare the incidence of ventilator-associated pneumonia between two groups of patients randomised to have closed system suction catheter changes every 24 hours and patients having closed system suction catheter changes every seven days or as required.
Status | Completed |
Enrollment | 344 |
Est. completion date | April 2004 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Aged greater than 18 years - Mechanically ventilated for more than 24 hours Exclusion Criteria: - Admitted from other hospital already mechanically ventilated - Massive haemoptysis - Previously received mechanical ventilation |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Australia | The Alfred Hospital | Melbourne | Victoria |
Lead Sponsor | Collaborator |
---|---|
Bayside Health | Deakin University |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | ventilator-associated pneumonia | |||
Secondary | length of hospital | |||
Secondary | intensive care stay | |||
Secondary | duration of mechanical ventilation | |||
Secondary | hospital mortality | |||
Secondary | number of acquired organ system derangements | |||
Secondary | cost of the closed system suction catheters |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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N/A |