Weaning Outcome From Invasive Mechanical Ventilation

June 30, 2021 updated by: Zujin Luo, Beijing Chao Yang Hospital

Weaning Outcome From Invasive Mechanical Ventilation: a Prospective, Observational Cohort Study

The main purpose of the present study was to explore the weaning failure rate from invasive mechanical ventilation and to identify risk factors of weaning failure.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • China
      • Beiling, China
        • Recruiting
        • Respiratory intensive care unit, Beijing Chao Yang Hospital Jingxi Campus
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients requiring endotracheal intubation and invasive mechanical ventilation

Description

Inclusion Criteria:

  • Requiring endotracheal intubation and invasive mechanical ventilation

Exclusion Criteria:

  • Duration of invasive mechanical ventilation < 48 hours；
  • Presence of tracheostomy；
  • Presence of upper airway obstruction.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Weaning failure rate
Time Frame: 3.5 years
3.5 years
Spontaneous breathing trial failure rate
Time Frame: 3.5 years
3.5 years
Extubation failure rate
Time Frame: 3.5 years
3.5 years

Secondary Outcome Measures

Outcome Measure
Time Frame
ICU mortality
Time Frame: 3.5 years
3.5 years
Hospital mortality
Time Frame: 3.5 years
3.5 years
ICU length of stay
Time Frame: 3.5 years
3.5 years
Hospital length of stay
Time Frame: 3.5 years
3.5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Beijing Chao Yang Hospital

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

July 1, 2013

Primary Completion (Anticipated)

December 1, 2023

Study Completion (Anticipated)

March 31, 2024

Study Registration Dates

First Submitted

December 1, 2016

First Submitted That Met QC Criteria

December 1, 2016

First Posted (Estimate)

December 5, 2016

Study Record Updates

Last Update Posted (Actual)

July 2, 2021

Last Update Submitted That Met QC Criteria

June 30, 2021

Last Verified

June 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • BeijingCYH-ICU-003

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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