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
| Type | Name | Description |
|---|---|---|
| DEVICE | Intellivent ASV | Automated 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.