Ignite Creation Date:
2024-10-26 @ 3:43 PM
Last Modification Date:
2024-10-26 @ 3:43 PM
Study NCT ID:
NCT06655805
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-10-22
Brief Title:
Registry for Automated Mechanical VEntilation in Adults
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Registry for Automated Mechanical VEntilation in Adults
Status:
RECRUITING
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
RAVE
Brief 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
Detailed Description:
The harmful effect of invasive mechanical ventilation can be prevented by intensive training of ICU physicians respiratory therapists and ICU nurses on the one hand and by improvement of the technology installed in ventilators on the other hand Advanced mechanical ventilation modes use new technologies to assist physiology optimize gas exchange and minimize ventilator induced lung injury Modes such as proportional assist ventilation and neuronally adjusted ventilatory assist deliver assisted ventilation proportional to the patients effort improving ventilator patient synchrony The Adaptive Support Ventilation ASV mode automatically adjust tidal volume and respiratory rate based on patients respiratory mechanics to protect from mechanical ventilator induced lung injury hence deliver safe mechanical ventilation The implementation of advanced closed-loop systems automates medical reasoning and has potential to improve patient ventilator interactions the time spent on mechanical ventilation staff workload and potentially outcome
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None