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Clinical Trials/ACTRN12619001075178
ACTRN12619001075178
Completed
未知

Effect of intrapulmonary percussive ventilation in spontaneously breathing non-ventilated patients in critical care on oxygenation, pulmonary complications and length of stay compared to standard chest physiotherapy: A randomised controlled trial

epean Hospital0 sites106 target enrollmentAugust 5, 2019

Overview

Phase
未知
Intervention
Not specified
Conditions
pulmonary atelectasis,
Sponsor
epean Hospital
Enrollment
106
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
August 5, 2019
End Date
December 24, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
epean Hospital

Eligibility Criteria

Inclusion Criteria

  • Age: adults greater than or equal to 16 years
  • \-FiO2 greater than or equal to 28% via mask or high flow nasal cannula or greater than or equal to 3 litres/minute via nasal cannula
  • \-Evidence of pulmonary atelectasis or consolidation (Confirmed by ICU clinician)
  • \-Patients with SpO2 less than or equal to 90% on room air (RA), respiratory rate (RR) greater than or equal to 25, accessory muscle use (with exception of chronic pulmonary or cardiac condition where a lower SpO2 range is acceptable by the medical team).
  • \-Evidence of sputum retention (based on cough assessment and auscultation findings)

Exclusion Criteria

  • Intubated patients
  • \-Hypoxemia due to non\-respiratory or non\-reversible causes such as congestive cardiac failure, low haemoglobin levels, pulmonary hypertension, pulmonary embolism
  • \-Hemodynamic instability; Systolic BP less than or equal to 80 mm Hg, acute myocardial ischemia, ventricular arrhythmia
  • \-FiO2 greater than or equal to 70%
  • \-Pneumothorax (with or without ICC)
  • \-Post esophagectomy / pneumonectomy patients
  • \-Patients with facial fractures/injuries/surgeries
  • \-Frank haemoptysis
  • \-Uncooperative/agitated/confused patients (RASS greater than or equal to \+2\)
  • \-Drowsy/sedated/unresponsive patients (RASS less than or equal to \- 2\)

Outcomes

Primary Outcomes

Not specified

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