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Clinical Trials/NCT05035355
NCT05035355
Unknown
Not Applicable

A Spontaneous Breathing Trial-based Protocol-directed Program in Difficult-to-Wean Patients

JinyanXing1 site in 1 country200 target enrollmentJanuary 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiration, Artificial
Sponsor
JinyanXing
Enrollment
200
Locations
1
Primary Endpoint
mechanical ventilation days
Last Updated
4 years ago

Overview

Brief Summary

Weaning patients from a ventilator is one of the most challenging processes in an intensive care unit. The investigators aimed to determine whether spontaneous breathing trial (SBT)-based protocol-directed weaning combined with the high-flow nasal cannula (HFNC) could be superior to routine SBT-based weaning in reducing the duration of mechanical ventilation (MV) in difficult-to-wean patients.

Registry
clinicaltrials.gov
Start Date
January 1, 2019
End Date
December 31, 2021
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
JinyanXing
Responsible Party
Sponsor Investigator
Principal Investigator

JinyanXing

Director

The Affiliated Hospital of Qingdao University

Eligibility Criteria

Inclusion Criteria

  • age ≥ 16 years old
  • MV for more than 48 hours
  • intubated or tracheostomized

Exclusion Criteria

  • pregnancy
  • irreversible respiratory failure caused by neurodegenerative disorders, such as Alzheimer disease, motor neuron disease, or multiple system atrophy
  • pre-existing decision to limit life support
  • waiving of MV during treatment
  • terminal stage of severe illness

Outcomes

Primary Outcomes

mechanical ventilation days

Time Frame: 60 days

the duration of mechanical ventilation

Secondary Outcomes

  • re-intubated within 24 hours(24 hours)

Study Sites (1)

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