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Breathing Pattern, WOB and Gas Exchange in Patients With Acute Respiratory Distress Syndrome During the Spontaneous Breathing Trial

Breathing Pattern, Work of Breathing and Gas Exchange in Patients With Acute Respiratory Distress Syndrome During the Spontaneous Breathing Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04209270
Enrollment
37
Registered
2019-12-24
Start date
2019-04-01
Completion date
2022-12-01
Last updated
2019-12-26

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

Conditions

ARDS, Weaning Failure, Work of Breathing

Brief summary

There is little evidence about the mechanical characteristics and muscular function in patients with Acute Respiratory Distress Syndrome (ARDS) at the time of weaning of the mechanical ventilation, as well as the behavior of the mechanical properties, breathing pattern, muscular effort, and gas exchange during a successful and failed spontaneous breathing trial.

Detailed description

The study of the respiratory system (RS) mechanics in patients with ARDS has been focused on the initial phase of ventilatory support, with few studies observing the weaning in mechanical ventilation.The RS in patients with ARDS is characterized by a greater or lesser degree of low functional residual capacity (FRC) in relation to normal. At the time of performing a spontaneous breathing trial, these mechanical characteristics determine the need to develop a high transpulmonary pressure during each breath, with high work of breathing (WOB) to achieve adequate alveolar ventilation. Inspiratory muscle weakness could alter the ability to generate the necessary transpulmonary pressure over time according to the loads imposed at the time of performing a spontaneous breathing trial, with the consequent development of fatigue and ventilatory failure. This is why the investigators propose to evaluate the association between elastic WOB and the failure of the spontaneous breathing trial.

Interventions

None listed

Sponsors

Sanatorio de la Trinidad Mitre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* over 18 years old * requiring mechanical ventilation for more than 12 hours * moderate/ severe ARDS according to Berlin Definition * able to make a Spontaneous Breathing Trial according to the institution protocol

Exclusion criteria

* pregnant patients * history of neuromuscular disease * patients in palliative care * bronchopleural fistula * contraindication of measurement of esophageal pressure

Design outcomes

Primary

MeasureTime frameDescription
Spontaneous breathing TrialDuring 60 minutes after inclusion or until the patient fails to breathe spontaneouslyPeriod of time in which the patient breathes spontaneously

Countries

Argentina

Contacts

Primary ContactEmilio Steinberg, RT
emi.stieinberg@gmail.com0054 91164977663
Backup ContactSebastian Fredes, RT
sebastian_fredes@hotmail.com

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026