Mechanical Ventilation Weaning

5

Review clinical trials related to Mechanical Ventilation Weaning. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

High Flow Tracheal Oxygen for Weaning of Tracheostomized Patients

In this pilot randomized controlled trial (RCT), the investigators aim to explore the feasibility of conducting a powered RCT that examines the efficacy and safety of high flow tracheal oxygen (HFTO) in weaning critically ill tracheostomy patients from mechanical ventilation. Objective of the study 1. To assess the feasibility of conducting a larger RCT as primary objective. 2. To explore the effect of using HFTO in mechanically ventilated tracheostomized critically ill patients on ventilator-free days (VFD) compared to standard of care method using tracheal mask (TM) as secondary objective.

Participants needed: 88
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: King Faisal Specialist Hospital & Research CenterUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Adults ≥ 18 years of age [+3]

Planned tracheostomy post head and neck surgery with ICU stay less than 48 hours [+4]

Status: Not yet recruiting

Phenotype-Guided Weaning in Mechanically Ventilated Patients With Chronic Comorbidities

The goal of this clinical trial is to learn whether a phenotype-guided weaning strategy can help adults with chronic comorbidities be liberated from invasive mechanical ventilation earlier. It will also learn about the safety of this strategy. The main questions it aims to answer are: * Does the phenotype-guided weaning strategy increase the number of ventilator-free days within 28 days after enrollment? * Does the strategy improve the process and success of ventilator liberation? * What safety events occur when this strategy is used? Researchers will compare the phenotype-guided weaning strategy with standard care in mechanically ventilated patients with chronic cardiovascular, cerebrovascular, or respiratory comorbidities. In the intervention period, participants will receive a protocolized ventilator weaning pathway. This pathway includes assisted ventilation transition, daily weaning readiness screening, a 0 cmH2O continuous positive airway pressure test, spontaneous breathing trial, extubation assessment, and post-extubation respiratory support when appropriate. The phenotype-guided part of the strategy is mainly used for participants who fail a spontaneous breathing trial or have difficult weaning. These participants will undergo structured ABCDE screening to identify the main phenotype or mechanism of weaning failure: * A: airway or lung dysfunction * B: brain dysfunction, including delirium, anxiety, agitation, or impaired consciousness * C: cardiac dysfunction * D: diaphragm or respiratory muscle dysfunction * E: endocrine, metabolic, or nutritional problems Based on the identified phenotype, clinicians will provide targeted assessment and treatment. Participants will be followed for ventilator-free days through day 28 and for clinical outcomes through day 90.

Participants needed: 1,380
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Southeast University, ChinaUpdated: May 19, 2026
Eligibility criteria

Age 18 years or older. [+4]

Severe neuromuscular disease, such as Guillain-Barre syndrome, myasthenia gravis... [+5]

Status: Not yet recruiting

The Use of Diaphragmatic Ultrasonography in Mechanical Ventilation Weaning Decision in COPD Patient

The aim of this study is to evaluate the use of diaphragmatic ultrasonography in taking mechanical ventilation weaning decision and predicting outcome in Chronic obstructive pulmonary disease patient. Primary outcome: • Number of patients with failed weaning trial and need reintubation. Secondary outcomes: * Time till extubation trial. * Ventilation free days after extubation less or more than 48h . * Number of Intensive care unit discharges. * Sensitivity and specificity of diaphragmatic assessment as a predictor of weaning.

Participants needed: 140
Trial details
Age: 21-70Biological sex: AllType: InterventionalSponsor: Tanta UniversityUpdated: Jul 24, 2025Locations: 1
Eligibility criteria

Adult patient more than 21 years old of both sexes, coming to our intensive care...

Patient refusal. [+4]

Status: Not yet recruiting

Feasibility Study to Compare Two Ventilatory Modes for Mechanical Ventilation Weaning

We hypothesize that the ventilatory mode Bilevel Positive Airway Pressure without any synchronization (BIPAPasynchro) may facilitate the weaning process of patients intubated with acute hypoxiemic respiratory failure (AHRF) by obviating the problem of patient-ventilator asynchrony. In order to prove this hypothesis a large randomized controlled study should be perfromed comparing BIPAPasynchro versus pressure support ventilation (PSV), the most widely used ventilatory mode during the weaning process. In order to do so, a feasibility trial to demonstrate the ICU personnel can effectively use a non-standard ventilatory mode should be first performed. The objective of our study is, thus, to demonstrate the feasibility of using BIPAasynchro in the Lausanne Adult ICU.

Participants needed: 84
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Lausanne HospitalsUpdated: Apr 15, 2025Locations: 2
Eligibility criteria

Intubated ICU patient with acute respiratory failure; [+5]

less than 18 years old; [+12]

Status: Not yet recruiting

Autonomic Modulation in Patients Undergoing Assisted Mechanical Ventilation: Comparison Between PAV+ and PSV

The aim of the study is to investigate autonomic modulation in terms of heart rate variability (i.e., HRV) in patients undergoing assisted mechanical ventilation in PSV mode, compared to patients assisted in PAV+ mode. The hypothesis is that the greater patient-ventilator synchrony of the latter mode may represent an advantage in reducing the imbalance of autonomic modulation.

Participants needed: 48
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of Roma La SapienzaUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

Patients admitted to the ICU, ≥18 years old, undergoing invasive controlled mech...

Successful completion of a spontaneous breathing trial (SBT) and spontaneous bre... [+9]