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Clinical Trials/NCT02687074
NCT02687074
Unknown
Not Applicable

Effects of High Flow Nasal Canula on Moderate and Severe Respiratory Failure Patients

Southeast University, China0 sites246 target enrollmentJanuary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Southeast University, China
Enrollment
246
Primary Endpoint
intubation rate on 28 days
Last Updated
10 years ago

Overview

Brief Summary

Respiratory failure is the danger for the patients admitted in ICU, mechanical ventilation could save a lot of patients' life, however, it prolongs patients' ICU stay and hospital stay. High flow nasal cannula (HFNC) has advantages of PEEP effects, reducing dead space, increasing EELV and improving comfort, and it has been used to treat respiratory failure patients. In recent study, HFNC could improve mortality of respiratory failure patients with P/F<200mmHg in the subgroup. The investigators want to start a randomized controlled study to evaluate the effects of HFNC on the patients with respiratory failure.

Detailed Description

just as the brief summary

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
December 2017
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Southeast University, China
Responsible Party
Principal Investigator
Principal Investigator

Chun Pan

Principal Investigator

Southeast University, China

Eligibility Criteria

Inclusion Criteria

  • Age\>18 years
  • patients met all four of the following criteria:
  • a respiratory rate of more than 25 breaths per minute,
  • a ratio of the partial pressure of arterial oxygen (Pao2) to the Fio2 of 300 mm Hg or less while the patient was breathing oxygen at a flow rate of 10 liters per minute or more for at least 15 minutes,
  • a partial pressure of arterial carbon dioxide (Paco2) not higher than 45 mmHg, and
  • an absence of clinical history of underlying chronic respiratory failure

Exclusion Criteria

  • Paco2 of more than 45 mm Hg
  • exacerbation of asthma or chronic respiratory failure
  • cardiogenic pulmonary edema
  • severe neutropenia
  • hemodynamic instability, use of vasopressors,
  • Glasgow Coma Scale score of 12 points or less (on a scale from 3 to 15, with lower scores indicating reduced levels of consciousness)
  • contraindications to noninvasive ventilation
  • urgent need for endotracheal intubation, a do-not-intubate order, and a decision not to participate.

Outcomes

Primary Outcomes

intubation rate on 28 days

Time Frame: up to 28 days

Secondary Outcomes

  • Duration of ICU stay(date of death from any cause, whichever came first, assessed up to 90 days)
  • Duration of hospital stay(date of death from any cause, whichever came first, assessed up to 90 days)

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