- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04735497
Ventilator Asynchrony as a Predictor of Weaning Failure
Patient Ventilator Asynchrony as a Predictor of Weaning Failure in Mechanically Ventilated COPD Patients
Study Overview
Status
Conditions
Detailed Description
Patient-ventilator asynchrony is defined as a lack of organization between the patient and ventilator timing of both inspiration and expiration . It is a commonly reported problem during mechanical ventilation. Thille et al. found that 24% of patients developed asynchrony in at least ten percent of their breaths, moreover they stated that the most frequent asynchronies was each of ineffective triggering and double triggering . Eighty percent of chronic obstructive pulmonary disease (COPD) patients experienced ineffective triggering, where it is considered the most frequent asynchrony in this group of patients. Asynchrony between Patient and ventilator also leads to prolonged duration of invasive ventilation, and increase possibility of weaning failure.
Both spread and intensity of asynchrony during the early phase of weaning in COPD patients has never satisfactorily described. The aim of the current study was to describe the patient-ventilator asynchrony and its impact on weaning outcome in mechanically ventilated COPD patients.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Assuit, Egypt, 71515
- Assuit University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
All COPD patients who were diagnosed after history ,physical examination radiology and pulmonary function tests and required mechanical ventilation.
Exclusion Criteria:
- Age < 18 years
- Tracheostomy
- Failure to trigger breaths even in cases of receiving neuromuscular blocking agents.
- Encephalopathy which is not caused by hypercapnia or hypoxemia either post arrest or due to cerebrovascular stroke
- Patients with unplanned weaning
COPD patients where intubation not related to exacerbation e.g. acute pulmonary edema.
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Failed Weaning
Patients who failed to be liberated from mechanical ventillation
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Successful Weaning
Patients who were liberated from mechanical ventillation and needed no respiratory support
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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To study effect of different types of ventilator asynchrony on weaning in mechanically ventilated COPD patients
Time Frame: One year
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Detection of patient ventilator asynchrony was done on 30-minute sessions following intubation by visual assessment of pressure, flow and volume graphs on ventilator .Repeated measures are done from the begining of mechanical ventilation and type of asynchronies including ineffective trigger double trigger, auto trigger , delayed cycle, early cycle and flow asynchrony. were recorded. |
One year
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Samiaa Sadek, Ass.Lecturer, Assiut University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Ventilator Asynchrony
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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