Clinical Trials Directory

Trials / Completed

CompletedNCT02651935

Intellivent ASV in Chronic Obstructive Pulmonary Disease Patients in the ICU

A Randomized Controlled Trial Comparing a Fully Closed Loop Ventilation Mode (Intellivent ASV) With Pressure Controlled + Pressure Support Ventilation in COPD Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Izmir Dr Suat Seren Chest Diseases and Surgery Education and Research Hospital · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This study will evaluate the effect of a fully closed loop ventilation mode (Intellivent ASV) on the duration of ventilation compared to conventional modes in COPD patients.

Detailed description

COPD patients often need invasive mechanical ventilation and due to the difficulties in the weaning of these patients, duration of mechanical ventilation can be relatively longer when compared with other ICU patients. Automated systems show promising results in shortening the weaning time in some patient groups. The aim of this study is to evaluate the effect of Intellivent-ASV with Quickwean function on the total duration of invasive mechanical ventilation as a primary outcome. Secondary outcomes are success rate and duration of weaning, ventilator free days at day 28 and intubation free days at day 28 (including NIV) when compared to conventional ventilation with t-piece weaning.

Conditions

Interventions

TypeNameDescription
DEVICEIntellivent ASVAutomated Invasive mechanical ventilation and weaning strategy

Timeline

Start date
2015-08-01
Primary completion
2019-02-01
Completion
2019-02-01
First posted
2016-01-11
Last updated
2021-07-29

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT02651935. Inclusion in this directory is not an endorsement.