RecruitingNCT06655805

Registry for Automated Mechanical VEntilation in Adults


Sponsor

Hamilton Medical AG

Enrollment

1,000 participants

Start Date

Sep 23, 2024

Study Type

OBSERVATIONAL

Conditions

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.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • Age ≥ 18 years. Any patient in need of HFNO, NIV and IMV at some time during its ICU stay.

Exclusion Criteria2

  • Expected to be weaned from HFNO, NIV within 2 hours. Expected to be weaned and extubated from IMV without subsequent need of HFNO or NIV support within 2 hours.
  • Expected to be transferred to another non-participating ICU within 2 hours. Moribund subject: death expected within 2 hours.

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Interventions

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

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


Locations(4)

HOCH Health Ostschweiz, Clinics for Intensive Care Medicine, Surgical ICU

Sankt Gallen, Canton of St. Gallen, Switzerland

Kantonsspital Chur

Chur, Kanton Graubünden, Switzerland

HOCH Health Ostschweiz, Clinics for Intensive Care Medicine, Medical ICU

Sankt Gallen, St.Gallen, Switzerland

Kantonsspital Winterthur, Zentrum für Intensivmedizin

Winterthur, Switzerland

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NCT06655805