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

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.

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

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.

Clinical Trials on Acute Respiratory Distress Syndrome

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