- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02881385
Effects on Respiratory Patterns and Patient-ventilator Synchrony Using Pressure Support Ventilation
September 10, 2016 updated by: Chun Pan, Southeast University, China
Effects on Respiratory Patterns and Patient-ventilator Synchrony in Different Ventilator Using Pressure Support Ventilation
Pressure Support Ventilation use Expiratory triggering sensitivity(Esense) to transfer inspiration to expiration,the value of Esense is fixed.That may lead to asynchrony between humans and ventilators,making people uncomfortable and prolonging weaning time.Some ventilators have auto cycle function Based on curves of pressure on respiratory patterns,it will make the transforming more synchrony with humans.Our prospective observational study will prove the superiority of the auto cycle function.
Study Overview
Status
Unknown
Detailed Description
From August 31st 2016 to August 31st 2017, all ARDS 、COPD and postoperative patients admitted to the ICUs will be enrolled.
The demographic characteristics, diagnosis, formerly medical history, Ventilator indications, Ventilator data, other respiratory treatments, weaning outcome and 28 day mortality will be recorded
Study Type
Observational
Enrollment (Anticipated)
45
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 to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
mechanical ventilation adult people using PSV mode in ICU
Description
Inclusion Criteria:
ARDS,COPD and Postoperative patient
Exclusion Criteria:
variety of reasons can not be placed next to the bed by the nasal EAdi catheter
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
Cohorts and Interventions
Group / Cohort |
|---|
|
E5 Esense 10%
PSV mode using E5 ventilator with Esense 10%
|
|
E5 Esense 30%
PSV mode using E5 ventilator with Esense 30%
|
|
E5 Esense 50%
PSV mode using E5 ventilator with Esense 50%
|
|
Servo-I Esense 10%
PSV mode using Servo-I ventilator with Esense 10%
|
|
Servo-I Esense 30%
PSV mode using Servo-I ventilator with Esense 30%
|
|
Servo-I Esense 50%
PSV mode using Servo-I ventilator with Esense 50%
|
|
E5 Esense autocycle
PSV mode using E5 ventilator with Esense Auto cycle
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
patient-ventilator synchrony using PSV mode between different ventilator for 180mins
Time Frame: 180mins after the patients involved
|
180mins after the patients involved
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Patient Respiratory Patterns during Pressure Support Ventilation for 180mins
Time Frame: 180mins
|
180mins
|
|
Patient gas exchange during Pressure Support Ventilation for 180mins
Time Frame: 180mins
|
180mins
|
|
Effects on Respiratory Patterns in different Expiratory triggering sensitivity for 180mins
Time Frame: 180mins
|
180mins
|
|
work of triggering and respiratory in different Expiratory triggering sensitivity for 180mins
Time Frame: 180mins
|
180mins
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
September 1, 2016
Primary Completion (Anticipated)
August 1, 2017
Study Completion (Anticipated)
August 1, 2017
Study Registration Dates
First Submitted
July 30, 2016
First Submitted That Met QC Criteria
August 23, 2016
First Posted (Estimate)
August 29, 2016
Study Record Updates
Last Update Posted (Estimate)
September 13, 2016
Last Update Submitted That Met QC Criteria
September 10, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- zhongdayiyuanICU
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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