Effects on Respiratory Patterns and Patient-ventilator Synchrony Using Pressure Support Ventilation

NCT ID: NCT02881385

Last Updated: 2016-09-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

45 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-09-30

Study Completion Date

2017-08-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Acute Respiratory Distress Syndrome COPD Post Operative

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CROSSOVER

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

E5 Esense 10%

PSV mode using E5 ventilator with Esense 10%

No interventions assigned to this group

E5 Esense 30%

PSV mode using E5 ventilator with Esense 30%

No interventions assigned to this group

E5 Esense 50%

PSV mode using E5 ventilator with Esense 50%

No interventions assigned to this group

Servo-I Esense 10%

PSV mode using Servo-I ventilator with Esense 10%

No interventions assigned to this group

Servo-I Esense 30%

PSV mode using Servo-I ventilator with Esense 30%

No interventions assigned to this group

Servo-I Esense 50%

PSV mode using Servo-I ventilator with Esense 50%

No interventions assigned to this group

E5 Esense autocycle

PSV mode using E5 ventilator with Esense Auto cycle

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Southeast University, China

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Chun Pan

physician

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

zhongdayiyuanICU

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.