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Clinical Trials/NCT01870765
NCT01870765
Completed
Not Applicable

Prospective Randomised Study on the Safety of Non-invasive Ventilation Versus High-flow Oxygen in Patients With Hypoxemic Respiratory Failure Undergoing Fiberoptic Bronchoscopy.

Universitätsklinikum Hamburg-Eppendorf1 site in 1 country40 target enrollmentJuly 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Enrollment
40
Locations
1
Primary Endpoint
Mean decrease in the saturation of oxygen (SpO2) during bronchoscopy.
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Bronchoscopy with broncho-alveolar lavage is a diagnostic tool in patients with pneumonia. Especially patients with acute or chronic pulmonary diseases are at risk of respiratory failure during or after bronchoscopy. It is known that in these cases bronchoscopy can be performed safely using non-invasive ventilation. It seems probable that high-flow oxygen, which is used in the treatment of patients with hypoxemic respiratory failure, is equally effective in preventing the development of respiratory failure during fiberoptic bronchoscopy while improving patient comfort. In this prospective randomised study the safety of high-flow oxygen is compared with non-invasive ventilation in patients with hypoxemic respiratory failure undergoing fiberoptic bronchoscopy.

Registry
clinicaltrials.gov
Start Date
July 2013
End Date
February 2014
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stefan Kluge

PD Dr. Stefan Kluge

Universitätsklinikum Hamburg-Eppendorf

Eligibility Criteria

Inclusion Criteria

  • patients treated in an intensive care unit
  • indication for bronchoscopy and broncho-alveolar lavage
  • presence of hypoxemic (SaO2/fraction of inspired oxygen(FiO2): 300 or less) and/or hypercapnic respiratory failure

Exclusion Criteria

  • patients already on invasive ventilation
  • indication for intubation
  • blocked nasopharynx
  • contraindications for non-invasive ventilation or high-flow oxygen

Outcomes

Primary Outcomes

Mean decrease in the saturation of oxygen (SpO2) during bronchoscopy.

Time Frame: during fiberoptic bronchoscopy

Secondary Outcomes

  • Changes in blood gases after the completion of fiberoptic bronchoscopy.(1 hour after the completion of bronchoscopy)

Study Sites (1)

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