Weaning From Mechanical Ventilation Guide by Assessment of Lung Tidal Distribution With EIT
1 other identifier
observational
55
1 country
1
Brief Summary
To evaluate whether EELI, RVD, GI were good predictor for weaning from mechanical ventilation
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2016
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 18, 2016
CompletedFirst Submitted
Initial submission to the registry
April 9, 2017
CompletedFirst Posted
Study publicly available on registry
April 18, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2018
CompletedNovember 30, 2022
November 1, 2022
2.2 years
April 9, 2017
November 28, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Weaning duration
Time of weaning duration from SBT to weaning from mechanical ventilation
48 hours
Study Arms (1)
Weaning Guide by EIT
Weaning From Mechanical Ventilation Guide by Assessment of Lung Tidal Distribution With EIT
Interventions
Changes of lung tidal distribution during SBT with mechanical ventilation were recorded by EIT can be used to predict weaning success or failure
Eligibility Criteria
Patients with mechanical ventilation admitted to ICU of Zhongda hospital
You may qualify if:
- Intubated patients age between 18 years old and 80 years old
- Duration of controlled mechanical ventilation≥ 24 h
- Patients ready to wean from mechanical ventilation
- Informed consent
You may not qualify if:
- Pregnant women
- Patients with malignant tumor
- High paraplegia, neuromuscular lesions
- Thoracic deformity, diaphragmatic hernia
- Patients with ECMO
- Patient participated in another interventional trial before enrollment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zhongda Hospital
Nanjing, Jiangsu, China
Study Officials
- PRINCIPAL INVESTIGATOR
Liu Songqiao, PHD
Southeast University
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
April 9, 2017
First Posted
April 18, 2017
Study Start
October 18, 2016
Primary Completion
December 31, 2018
Study Completion
December 31, 2018
Last Updated
November 30, 2022
Record last verified: 2022-11
Data Sharing
- IPD Sharing
- Will not share