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Prophylaxis of Ventilator Associated Pneumonia by Continuous Lateral Rotation Therapy

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Medical University of Vienna

Status

Completed

Conditions

Pneumonia, Ventilator-Associated

Treatments

Procedure: Continuous lateral rotation therapy

Study type

Interventional

Funder types

Other

Identifiers

NCT00529776
EK 38/2004

Details and patient eligibility

About

Hypothesis: Ventilator associated pneumonia (VAP) in critically ill patients may be prevented by continuous lateral rotation therapy (CLRT) using specially designed, motor driven beds.

Patients are randomized to CLRT or supine position if mechanically ventilated and not suffering from pneumonia or ARDS within 48 hours after intubation. Prophylaxis of VAP is standardized in both groups. Primary endpoint is incidence of VAP, secondary endpoints are length of ventilation, length of stay and mortality.

Enrollment

150 patients

Sex

All

Ages

18 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Mechanically ventilated
  • Intubated not longer than 48 h
  • Medical cause for ICU admission
  • Expected to be ventilated for > 48 hours

Exclusion criteria

  • Pneumonia or ARDS present
  • Postoperative patient

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

150 participants in 2 patient groups

1
Active Comparator group
Description:
Continuous lateral rotation therapy
Treatment:
Procedure: Continuous lateral rotation therapy
2
No Intervention group
Description:
Standard manual positioning (Supine position)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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