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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00447109
Other study ID # 122/02
Secondary ID T10308
Status Completed
Phase N/A
First received March 12, 2007
Last updated March 13, 2007
Start date September 2003
Est. completion date April 2004

Study information

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

Clinical Trial Summary

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.


Description:

Comparison(s): 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.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Intervention

Device:
Closed system suction


Locations

Country Name City State
Australia The Alfred Hospital Melbourne Victoria

Sponsors (2)

Lead Sponsor Collaborator
Bayside Health Deakin University

Country where clinical trial is conducted

Australia, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT00542321 - Pilot Study of Lateral Rotation Interventions for Efficacy and Safety in ICU Care N/A