Mechanical Power under Closed-loop versus Conventional Ventilation - a multicenter crossover randomized clinical trial.

Completed

• Conditions: respiratory insufficiency; 10024967

• Registration Number: NL-OMON52209
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 84

Inclusion Criteria

• Admitted to one of the participating ICUs;
• Receiving invasive ventilation through a standard endotracheal tube;
• Expected to be ventilated > 24 hours;
• Ventilation with a ventilator that provides INTELLiVENT-ASV.

Exclusion Criteria

• Age under 18 years of age;
• No written informed consent;
• Morbidly obese;
• Any contra-indications for use of INTELLiVENT-ASV

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is the amount of MP with each form of invasive<br /><br>ventilation.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>N.a.</p><br>