Prone Craniotomy, Endotracheal Intubation Fixation
Conditions
Brief summary
The aim of this randomized controlled trial is to evaluate the clinical effects of trans-nasal ETT fixation for prone ventilation.
Interventions
DEVICESFC
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 .
Sponsors
China Medical University, China
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No
Inclusion criteria
* age 18-60 years old, * ASA grade Ⅰ-Ⅱ, * 18\<BMI\<24.
Exclusion criteria
* the intubation time was less than 5 hours, * oral and facial skin damage, * allergic to adhensive tapes, * nasotracheal intubation, * patients were edentulous.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| the distance of tube movement | 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. |
Countries
China
Outcome results
None listed