Alveolar recruitment manoeuvre
ProcedureIncrease airway pressure during pressure controlled ventilation up to peak-airway pressure of 40 cmH20 and PEEP of 15 cmH20.
NCT Number: NCT00779090
In ventilated patients open endotracheal suctioning may lead to alveolar derecruitment, which can be monitored by means of functional residual capacity (FRC) measurements. The investigators hypothesized that a recruitment strategy based on FRC measurements would improve oxygenation and regional ventilation after an open endotracheal suctioning manoeuvre.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 4
In mechanically ventilated patients the functional residual capacity will be measured before (baseline) and after an open endotracheal suctioning manoeuvre. Based on these changes patients will be divided into two groups: Group A with more than 94% of baseline FRC, and Group B with less than 94% of baseline FRC. Both groups will be randomized to receive an alveolar recruitment manoeuvre or no alveolar recruitment manoeuvre, leading to four groups. Oxygenation and regional ventilation with electrical impedance tomography will be studied.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Increase airway pressure during pressure controlled ventilation up to peak-airway pressure of 40 cmH20 and PEEP of 15 cmH20.
Time frame: 60 minutes
Time frame: 60 minutes
University of Luebeck
Other
The Influence of a Functional Residual Capacity Guided Alveolar Recruitment Strategy After Open Endotracheal Suctioning on Oxygenation and Regional Ventilation
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT04014920
Body Weight, Intensive Care Unit
Montpellier, Herault, France
View Trial DetailsNCT07291271
Ablation Techniques, Adenocarcinoma
Amsterdam, Netherlands
View Trial DetailsNCT03657368
Orthopedic Surgery, Pathologic Processes
Cleveland, Ohio, United States
View Trial DetailsNCT04376918
Pathologic Processes, Pathological Conditions, Signs and Symptoms
Jerusalem, Israel
View Trial Details