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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.


Clinical Trial 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. ;


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00447109
Study type Interventional
Source Bayside Health
Contact
Status Completed
Phase N/A
Start date September 2003
Completion date April 2004

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