Automatic Detection of Dyspnea in Mechanically Ventilated, Critically Ill Patients
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorHospital de Clinicas José de San Martín
About this trial
The investigators will conduct a prospective, observational, two-center ICU study of 60 subjects on mechanical ventilation with respiratory failure of any cause.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults of either sex (≥18 years)
Endotracheally intubated in the past 24 hours.
Expected to require ≥24 hours of mechanical ventilation.
Disqualifiers
Continuous neuromuscular blockade.
Ventilated on Airway Pressure Release Ventilation mode.
Trial population
Adults of either sex with respiratory failure of any cause on invasive mechanical ventilation.
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
60 Participants
are grouped into 1 trial groupGroup A: Adults on invasive mechanical ventilation
Trial outcomes
Primary outcomes
1
Correlation between the pressure-time-product of inspiratory effort and the MV-RDOS score.
The degree of correlation between the pressure-time-product of inspiratory effort and the MV-RDOS score will be determined with Pearson's coefficient of determination (R2).
Time frame
One yearSecondary outcomes
1
Ventilator free days.
The number of days from the last day of invasive mechanical ventilation to day 28.
Time frame
One yearLocations
1Map coordinates are unavailable for these locations. Locations are shown below instead.
Hospital de Clínicas de la Universidad de Buenos AiresRecruiting Buenos Aires, Buenos Aires
Argentina
ArgentinaSponsors and contacts
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Source ClinicalTrials.gov