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Asynchrony During Mechanical Ventilation in Patients With Acute Respiratory Distress Syndrome

Asynchrony During Mechanical Ventilation in Patients With Acute Respiratory Distress Syndrome

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02732041
Enrollment
103
Registered
2016-04-08
Start date
2016-05-25
Completion date
2019-02-28
Last updated
2020-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Distress Syndrome, Adult, Ventilator-Induced Lung Injury

Brief summary

Asynchrony during mechanical ventilation has been poorly described in patients suffering from acute respiratory distress syndrome. The purpose of this study is to describe the frequency of asynchronies (ineffective efforts and double triggering) in these group and evaluate potential risk factors and prognosis implications.

Detailed description

Major patient-ventilator asynchronies have been described during assisted mechanical ventilation in different settings. Few studies have evaluated double cycling in ARDS patient. No clear predictors of this finding beside low tidal volume have been found, and clinical outcome implications have not been addressed. This study has 3 main objectives: evaluate the frequency of double cycling and ineffective efforts, seek for potential predictors and clinical outcomes related to asynchronies. Subjects with less than 72 hours of mechanical ventilation due to ARDS will be recruited. Thirty minutes of mechanical ventilation will be recorded and automatically analyzed with a custom-made program to detect asynchronies. A blood sample will be drawn to measure inflammatory and lung tissue damage biomarkers. Clinical and outcome data will be recorded.

Interventions

None listed

Sponsors

Centro de Educación Medica e Investigaciones Clínicas Norberto Quirno
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Acute Respiratory Distress Syndrome according to Berlin definition * Intubation and mechanical ventilation within 72 hours of inclusion

Exclusion criteria

* Known severe neuromuscular disease * Continuous neuromuscular blocking agents infusion

Design outcomes

Primary

MeasureTime frameDescription
Asynchrony rate30 minutesAsynchronies per minutes of mechanical ventilation

Secondary

MeasureTime frame
Length of mechanical ventilationFrom the date of intubation to the date of complete weaning from mechanical ventilation or death which ever comes first, up to 90 days
ICU mortalityFrom the date of admission to the date of discharge from the ICU, up to 90 days
Hospital mortalityFrom the date of admission to the date of discharge from the ICU, up to 90 days

Countries

Argentina

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026