Reverse Trigger Phenotypification and Response to Ventilatory Adjustments

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorHospital Civil de Guadalajara

About this trial

The goal of this prospective observational study is to describe the incidence of reverse trigger (RT) in mechanically ventilated patients with diagnosis of acute respiratory distress syndrome (ARDS).

The main questions it aims to answer are:

* Real incidence of RT based on continuous monitoring * The response to mechanical ventilatiory adjustments Participants will be included as soon as neuromuscular blockers (NMB)/sedation is stopped or in case of spontaneous respiratory efforts detection, whatever happens first. Continuous monitoring will be performed by esophageal manometry until switch to a pressure support (spontaneous) mode, restart of deep sedation/neuromuscular blockers by medical indication, or death.

In order to allow detection of possible RT in patients with ongoing sedation/NMB, mechanical ventilator waveforms will be screened every 1-2 hours by investigators and critical care physicians with at least 1 year of specific training in detection of dyssynchronies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Diagnosis of ARDS according to the Berlin criteria and added New Global Definition 2023

Mechanical ventilation

Disqualifiers

<18 years

Tracheostomy status

Pneumothorax

Tube thoracostomy with air leaks

Trial population

Mechanically ventilated patients with acute respiratory distress syndrome.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Incidence of reverse trigger

Proportion of patients who developed reverse trigger

Time frame
60 days

Secondary outcomes

1

Days of mechanical ventilation

Days of mechanical ventilation

Time frame
60 days
2

ICU length of stay

Days from ICU admission to discharge to wards

Time frame
60 days
3

Mortality

Rate of deceased patients in percentage

Time frame
60 days

Other outcomes

1

Duration of RT

Total time of presence of RT

Time frame
60 days
2

Phenotypes of RT

Rate of the different phenotypes according to cycle initiation and termination of patient's respiratory effort

Time frame
60 days
3

Intensity of breathing efforts

Intensity of respiratory efforts as measured by esophageal manometry

Time frame
60 days
4

Association with severity

Association of RT with lung disease severity as measured by pO2:FiO2 ratio

Time frame
60 days

Sponsors and contacts

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