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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06042036
Other study ID # 28482720.0.1001.0068
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 12, 2023
Est. completion date October 12, 2024

Study information

Verified date September 2023
Source University of Sao Paulo General Hospital
Contact Fabia D Silva, PhD
Phone 34992484248
Email fabiadiniz@usp.br
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study is to estimate the prevalence of the use of protective ventilation with low tidal volume ventilation in the transition of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure in ICUs in Latin America and its association with patient outcomes. The main questions it aims to answer are: - what is the prevalence of the use of low tidal volume ventilation (VT <8 mL/kg of predicted body weight) in the first 24 hours of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure? - Is there an association between the rate of adherence to low tidal volume ventilation in spontaneous ventilation modes and the ability to stay off ventilatory support and mortality? Participants are patients with acute respiratory failure under mechanical ventilation. Investigators will collect data on the ventilatory parameters of participants - 24 hours before they begin to be ventilated with spontaneous modes of ventilation - during the first 24 hours of spontaneous ventilation Investigators will collect several patient-centered clinical outcomes at 28 days after study inclusion, including ventilator-free days and mortality


Description:

Investigators will conduct a cohort study in Intensive Care Units (ICUs) across Latin America, aiming to include 422 patients with Hypoxemic Acute Respiratory Failure (ARF) and under invasive mechanical ventilation. The goal of this observational study is to estimate the prevalence of the use of protective ventilation with low tidal volume ventilation in the transition of spontaneous ventilation modes in patients with hypoxemic acute respiratory failure in ICUs in Latin America The primary objectives are to determine the prevalence of low tidal volume ventilation (VT < 8 mL/kg of predicted body weight) during the initial 24 hours of spontaneous ventilatory modes in patients diagnosed with hypoxemic ARF and its association with clinically important patient outcomes. Investigators are interested in assessing the rate of adherence to low tidal volume ventilation, defined as maintaining VT < 8 mL/kg of predicted body weight during the first 24 hours of ventilation in spontaneous mode.They are also interested in measuring the number of days that patients are alive and not receiving ventilatory support and survival at 28 days. Investigators will also measure the proportion of patients experiencing significant asynchrony during the transition to spontaneous mechanical ventilation, who revert to sedation and controlled mechanical ventilation within the first 24 hours or at any point during mechanical ventilation.


Recruitment information / eligibility

Status Recruiting
Enrollment 422
Est. completion date October 12, 2024
Est. primary completion date June 12, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 110 Years
Eligibility Inclusion Criteria: - Age > 18 years - Patients with hypoxemic ARF, defined as a PaO2/FIO2 ratio <300 mmHg, under controlled invasive mechanical ventilation, with an expected duration of MV of at least 24h. - Patients transitioning to spontaneous ventilation modes (PSV, PAV Plus, NAVA or APRV) Exclusion Criteria: - Tracheostomized patients. - Decision not to maintain or add life support measures on the day of assessment (palliative care). - Patient in ECMO. - Air fistula or barotrauma that prevents adequate tidal volume monitoring. - Severe injuries to the central nervous system that result in abolished or very high respiratory drive, for whom it is not possible to maintain protective tidal volume.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Spontaneous mode of mechanical ventilation
any mode of mechanical ventilation classified as spontaneous or proportional, mainly pressure support ventilation, but also CPAP, APRV, NAVA, PAV+

Locations

Country Name City State
Argentina Sanatorio Juncal SA Buenos Aires
Bolivia Hospital Municipal Boliviano Holandés, Universidad Mayor de San Andrés La Paz
Brazil Hospital das Clínicas -HCFMUSP Sao Paulo SP
Chile Pontificia Universidad Catolica de Chile Santiago
Colombia Clinica Universidad de la Sabana Chía
Ecuador Hospital Eugenio Espejo Quito
Mexico Hospital Civil Fray Antonio Alcalde Guadalajara
Paraguay Hospital San Roque Asunción
Peru Hospital Rebagliati Lima
Uruguay Hospital Espanol Montevideo

Sponsors (3)

Lead Sponsor Collaborator
University of Sao Paulo General Hospital Brazilian Research In Intensive Care Network, Latin American Intensive Care Network (LIVEN)

Countries where clinical trial is conducted

Argentina,  Bolivia,  Brazil,  Chile,  Colombia,  Ecuador,  Mexico,  Paraguay,  Peru,  Uruguay, 

Outcome

Type Measure Description Time frame Safety issue
Primary Low tidal volume Low tidal volume, defined as less or equal to 8 mLs per Kg of predicted body weight 24 hours
Primary Ventilator- free days number of days alive and not receiving invasive mechanical ventilation after transition to spontaneous ventilation 28 days
Secondary Hospital mortality mortality in the hospital 28 days
Secondary Rate of patient-ventilator asynchrony presence of patient asynchrony 24h after transition to a spontaneous mode of mechanical ventilation 24 hours
Secondary Number of participants that return to controlled mechanical ventilation in the first 24 hours return to controlled mechanical ventilation in the first 24 hours after transition to spontaneous ventilation 24 hours
Secondary Number of participants that return to sedation in the first 24 hours return to sedation in the first 24 hours after transition to spontaneous ventilation 24 hours
Secondary Number of participants that return to controlled mechanical ventilation after transition to spontaneous ventilation return to controlled mechanical ventilation any time after transition to spontaneous ventilation 28 days
Secondary Number of participants that return to sedation after transition to spontaneous ventilation return to sedation any time after transition to spontaneous ventilation 28 days
Secondary Number of participants with PEEP and FIO2 compatible with the ARDSnet PEEP/FIO2 table adherence to ARDSnet low PEEP/FIO2 table after transition to spontaneous ventilation 24 hours
Secondary Number of participants who were extubated Extubation and discontinuation of mechanical ventilation after the transition to spontaneous mode 28 days
Secondary Rate of reintubation Reintubation after transition to spontaneous mode and extubation 28 days
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