Tracheobronchial Secretion Removal
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00932776|
Recruitment Status : Completed
First Posted : July 3, 2009
Last Update Posted : July 3, 2009
|Condition or disease||Intervention/treatment||Phase|
|Respiration, Artificial Respiratory Insufficiency||Device: TBA care device Device: Control||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
Device: TBA care device
Tracheal suction maneuvers are performed according to the indications provided by the TBA care device or to clinical parameters whichever occurs first.
|Active Comparator: Control||
In this group suction maneuvers are performed according to clinical indications or on a fixed schedule whichever comes first.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00932776
|A.O. San Gerardo|
|Monza, MB, Italy, 20052|