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Registry for Automated Mechanical VEntilation in Adults

NCT06655805 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-01-16

No results posted yet for this study

Summary

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

  • Respiratory Insufficiency Requiring Mechanical Ventilation

Interventions

DEVICE

Non-invasive ventilation, Invasive mechanical ventilation, high-flow nasal oxygen

No intervention is intended by the nature of this observational study.

Sponsors & Collaborators

  • Hamilton Medical AG

    lead INDUSTRY

Principal Investigators

  • Francesca Porta, MD · Kantonsspital Chur, Chur, Switerzland 7000

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-23
Primary Completion
2030-06-30
Completion
2030-12-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06655805 on ClinicalTrials.gov