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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03250416
Other study ID # ChongqingMU2
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2017
Est. completion date September 30, 2021

Study information

Verified date July 2022
Source Chongqing Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

The investigator aimed to manage noninvasive ventilation in patients with hypoxemic respiratory failure.


Description:

Patients with hypoxemic respiratory failure were enrolled in this study. The investigator collected the data at beginning and first stage of noninvasive ventilation to analyze the efficacy of noninvasive ventilation. To manage the noninvasive ventilation easily, the investigator also aimed to develop a scale to predict the efficacy of noninvasive ventilation, and used this scale to guide clinicians how to use noninvasive ventilation.


Recruitment information / eligibility

Status Completed
Enrollment 2179
Est. completion date September 30, 2021
Est. primary completion date September 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - PaO2/FiO2 less than 300; PaCO2 less than 50 mmHg; Respiratory rate more than 25 breaths/min or presence of labored breath. Exclusion Criteria: - Requirement of emergency intubation; Sequential use of noninvasive ventilation after extubation;Use of noninvasive ventilation after accident extubation.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China The First Affiliated Hospital ,Chongqing Medical Univercity Chongqing Chongqing

Sponsors (1)

Lead Sponsor Collaborator
Chongqing Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Noninvasive ventilation failure Noninvasive ventilation failure was defined as requirement of intubation. From participation to 30 days
Secondary Mortality Mortality in ICU and hospital From participation to 30 days
Secondary ICU stay Length of ICU stay From participation to 30 days
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