Yue Yun
Shenyang, Liaoning, 110001, China
NCT Number: NCT05093595
The aim of this randomized controlled trial is to evaluate the clinical effects of trans-nasal ETT fixation for prone ventilation.
Looking for future studies?
Notify Me18 year–60 year
All sexes
Interventional
Not applicable
Shenyang, Liaoning, 110001, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The lubricated SFC passed nasally into the oropharynx under the visual guidance of visual laryngoscope to ensure that the cuff had passed through the posterior choanae and reached the oropharynx. The guide wire is removed and the balloon inflated with 5 ml normal saline. The catheter is then pulled slightly until the balloon is fixed and concealed by the soft palate . The ETT is anchored to the SFC with a cable tie .
Time frame: The participants will be followed from intubation to extubation, an expected average of 6 hours.
It is the difference between the preoperative depth of the supine tracheal tube and the postoperative depth of the prone tracheal tube.
China Medical University, China
Other
Trans-nasal ETT Fixation
Acronym: Trans
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.
NCT07390162
Adult Patients, Endotracheal Intubation Fixation
View Trial Details