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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01280019
Other study ID # FRC-ARF
Secondary ID
Status Recruiting
Phase Phase 4
First received January 19, 2011
Last updated January 19, 2011
Start date October 2010
Est. completion date May 2012

Study information

Verified date January 2011
Source University of Luebeck
Contact Hermann Heinze, MD
Email Hermann.heinze@uk-sh.de
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

In ventilated patients with acute respiratory failure endotracheal suctioning may lead to alveolar derecruitment, which can be monitored by means of functional residual capacity (FRC) measurements. Regional distribution of ventilation can be followed at bedside using electrical impedance tomography. The investigators hypothesize that a FRC guided recruitment strategy, aimed at restoring a baseline FRC value after open endotracheal suctioning, improves oxygenation and regional distribution of ventilation. In addition the investigators research the impact of such a strategy on the inflammatory response to mechanical ventilation.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date May 2012
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- need for mechanical ventilation due to respiratory failure after cardiac surgery

Exclusion Criteria:

- circulatory failure, eg. need for high doses of inotropes or extracorporal cardiac support

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care


Related Conditions & MeSH terms


Intervention

Procedure:
alveolar recruitment manoeuvre
Increase of airway pressures in a stepwise manner from set peak inspiratory pressure/ positive end-expiratory pressure up to 40/15 mbar and back over 2 minutes.

Locations

Country Name City State
Germany Department of Anaesthesiology, Intensive Care Unit, University of Lübeck Lübeck

Sponsors (2)

Lead Sponsor Collaborator
University of Luebeck European Society of Intensive Care Medicine

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Regional ventilation Regional distribution of ventilation over 6 hours of treatment 6 hours No
Secondary arterial oxygenation and inflammation Changes of arterial oxygenation and inflammatory parameters in the blood during 6 hours of treatment 6 hours No
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