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the Effect of Trans-nasal Fixation of Endotracheal Tubes for Prone Ventilation

C

China Medical University, China

Status

Completed

Conditions

Endotracheal Intubation Fixation
Prone Craniotomy

Treatments

Device: SFC

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this randomized controlled trial is to evaluate the clinical effects of trans-nasal ETT fixation for prone ventilation.

Enrollment

30 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

30 participants in 2 patient groups

Group A
No Intervention group
Description:
The tracheal tube was routinely fixed with a teeth pad and adhesive tape (3M).
Group B
Experimental group
Description:
The tracheal tube was fixed by the trans-nasal Silicone Foley Catheter (SFC) and adhesive tape.
Treatment:
Device: SFC

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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