Respiratory Mechanics Assessment During Assisted Mechanical Ventilation
NCT ID: NCT05203536
Last Updated: 2025-05-30
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
298 participants
OBSERVATIONAL
2021-09-01
2023-06-03
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Third International Study on Mechanical Ventilation
NCT01093482
Assessment of Lung Mechanics in COVID-19 Acute Respiratory Distress Syndrome
NCT04597853
Assessing Diaphragm Muscle Inactivity in Mechanically Ventilated ICU Patients
NCT02434016
Bed Side Assessment in Patients With Acute Respiratory Failure Under Invasive Mechanical Ventilation
NCT07265882
Effects of Invasive Mechanical Ventilation on the Right Ventricular Function
NCT05710419
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Invasive mechanical ventilation in one of these modes: Pressure A/C, PRVC, SIMV PC, PSV, NAVA, PAV+, BiPAP
* Presence of spontaneous breathing activity (ventilator triggering), since 6 hours and no longer than 48 hours
* Patient for full active management at this point.
Exclusion Criteria
* Pregnancy
* Active air leaks
* Moribund state
* High ICP
* Patient has passed a spontaneous breathing trial (if performed for clinical indication)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Milano Bicocca
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Toronto General Hospital
Toronto, Toronto, Canada
University Medical Centre Schleswig-Holstein
Kiel, Kiel, Germany
University Hospital Galway
Galway, Galway, Ireland
Ospedale Sant'Anna
Ferrara, Ferrara, Italy
Policlinico di Milano Ospedale Maggiore
Milan, Milano, Italy
ASST-Monza, Ospedale San Gerardo
Monza, Monza, Italy
Vall d'Hebron University Hospital
Barcelona, Barcelona, Spain
Hospital Clinic de Barcelona
Barcelona, Barcelona, Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
3552
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.