Actively Recruiting
Registry for Automated Mechanical VEntilation in Adults
Led by Hamilton Medical AG · Updated on 2026-01-16
1000
Participants Needed
4
Research Sites
327 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the here proposed study is to assess safety, performance and provide real world evidence (RWE) of the Hamilton Medical AG automated mechanical ventilation software packages in consecutive critically ill patients admitted to the intensive care unit.
CONDITIONS
Official Title
Registry for Automated Mechanical VEntilation in Adults
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Patients requiring high-flow nasal oxygen, non-invasive ventilation, or invasive mechanical ventilation during ICU stay
You will not qualify if you...
- Expected to be weaned from high-flow nasal oxygen or non-invasive ventilation within 2 hours
- Expected to be extubated from invasive mechanical ventilation without further support within 2 hours
- Expected transfer to a non-participating ICU within 2 hours
- Moribund patients with death expected within 2 hours
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 4 locations
1
HOCH Health Ostschweiz, Clinics for Intensive Care Medicine, Surgical ICU
Sankt Gallen, Canton of St. Gallen, Switzerland, 9007
Actively Recruiting
2
Kantonsspital Chur
Chur, Kanton Graubünden, Switzerland, 7000
Actively Recruiting
3
HOCH Health Ostschweiz, Clinics for Intensive Care Medicine, Medical ICU
Sankt Gallen, St.Gallen, Switzerland, 9007
Actively Recruiting
4
Kantonsspital Winterthur, Zentrum für Intensivmedizin
Winterthur, Switzerland, 8400
Actively Recruiting
Research Team
M
Marco V Maggiorini, MD
CONTACT
D
Dominik Novotni, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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