Weaning Failure Clinical Trial
Official title:
Weaning With Smartcare in Mechanically Ventilated Patients in the ICU - a Controlled and Randomized Study
Mechanical ventilation is widely used for ICU patients as a lifesaving procedure. However, it is associated with several complications, such as ventilator-associated pneumonia and the increase of hospital morbidity and mortality. To avoid such complications, we need to wean these patients off the ventilator as soon as possible. This must however be done at the right time to avoid other complications, such as the need for re-intubation. For this reason, it is important to have a specific weaning protocol, which will reduce the time on mechanical ventilation, and avoiding the need for re-intubation and other complications. Recently, an argument has developed as to which weaning protocol would be more appropriated, and whether a computer driven weaning protocol could have better results than the conventional weaning protocols focusing on daily screening and daily interruption of sedation followed by a spontaneous breathing test. Our objective is to compare mechanical ventilation times, weaning success up to 48 hours after extubation, re-intubation rates between a group with computer driven weaning protocol (SmartCare) versus a weaning protocol with daily weaning screens and spontaneous breathing trials in ICU patients ventilated for more than 24 hours.
Background: Mechanical ventilation (MV) weaning is commonly performed using Spontaneous
Breathing Trials (SBT) with pressure support ventilation after a daily weaning screen [1].
Recently there has been an increased interest in automatic weaning trials, which consists of
closed-loop ventilation, using ETCO2 monitoring during SBT [1, 2]. So far, there has been no
clinical evidence to compare automatic weaning trials with those of SBT.
Objective: To compare MV weaning times between an Automatic Weaning Ventilation System
(SmartCare/PS) and SBT groups.
Methods: A randomized, controlled study performed at a general ICU. Adult patients were
enrolled who were ventilated for more than 24 hours. Tracheostomies patients, those with
neurological conditions, and a Glasgow coma scales lower than 10 were excluded. Patients
were randomized to either the control or Smart Care group. All patients were ventilated with
a Drager Evita XL (Drager Medical, Lubeck, Germany) ventilator with SmartCare/PS software
version 1.1 available for use immediately prior to randomization. The Control group
consisted of a daily weaning screen and SBT with pressure support ventilation. If patients
tolerated SBT, they were extubated. Smart Care group patients were also submitted to a daily
weaning screen, after which they were ventilated with the SmartCare/PS mode. MV and weaning
time, maximum inspiratory pressure (MIP), maximum expiratory pressure (MEP), vital capacity
(VC), respiratory frequency to tidal volume ration (f/Vt), use of non-invasive ventilation
(NIV) post extubation, and re-intubation rate we evaluated.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05539599 -
Comprehensive Ultrasound Evaluation as a Predictor of Weaning
|
||
Completed |
NCT02845076 -
Weaning From Noninvasive Ventilation
|
N/A | |
Completed |
NCT01915563 -
Rest After Spontaneous Breathing Trial for Prevention of Post-extubation Failure
|
N/A | |
Recruiting |
NCT01721434 -
Effects of Levosimendan on Diaphragm Function in Mechanically Ventilated Patients
|
Phase 2/Phase 3 | |
Completed |
NCT01928277 -
Weaning From Mechanical Ventilation: Spontaneous Breathing Trial and the Assessment of Work of Breathing
|
N/A | |
Recruiting |
NCT05632822 -
Value of Diaphragm Function Predicting Weaning From Mechanical Ventilation
|
||
Completed |
NCT03240263 -
Inspiratory Muscle Training in Difficult to Wean Patients
|
N/A | |
Completed |
NCT06332768 -
NIV Versus HFO Versus Standard Therapy Immediately After Weaning From Mechanical Ventilation in ARDS Patients
|
N/A | |
Completed |
NCT01867853 -
Volume Responsiveness Before SBT Predicts the Outcome of Mechanical Ventilation Weaning in Critically Ill Patients
|
N/A | |
Recruiting |
NCT06040138 -
Monitoring of Breathing Effort Through Pressure Time Product Measurement Using Airway Occlusion Pressure
|
||
Completed |
NCT06224010 -
Respiratory Drive and Inspiratory Effort in COVID-19 Associated ARDS
|
||
Completed |
NCT03129217 -
The Validity of Maximal Diaphragm Thickening Fraction to Measure Diaphragm Function in Mechanically Ventilated Patients
|
||
Completed |
NCT05550220 -
A Modified Cuff Leak Test and Reintubation in Mechanically Ventilated Patients
|
N/A | |
Not yet recruiting |
NCT05431036 -
Evaluation of a Combined Model in Predicting Weaning Outcome in Critically Ill Patients.
|
||
Recruiting |
NCT05906888 -
Weaning With Tracheostomy - an Observational Study on Patient-centered Outcomes
|
||
Recruiting |
NCT05944588 -
Predictive Value of Chest Ultrasound Observation on Extubation Failure
|
||
Not yet recruiting |
NCT05802745 -
P0.1 and Extubation Failure in Critically Ill Patients
|
||
Recruiting |
NCT03894189 -
The Effect of Doxapram Versus Theophylline on Diaphragmatic Function
|
N/A | |
Completed |
NCT01877850 -
Utility of a Weaning Protocol in ICU
|
N/A | |
Completed |
NCT03580720 -
Electromyography for Diaphragm Effort
|
N/A |