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The Effectiveness of Using Bougie or Cooled Nasogastric Tube to Facilitate Nasotracheal Intubation

Using Bougie or Cooled Nasogastric Tube to Facilitate Nasotracheal Tube Advancement Into Trachea Under Video-laryngoscope

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04087837
Enrollment
90
Registered
2019-09-12
Start date
2019-06-14
Completion date
2020-12-31
Last updated
2021-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intubation Complication

Keywords

bougie, nasotracheal tube, Endotracheal Tube intubation General Anesthesia (ETGA)

Brief summary

either uses a bougie or nasogastric tube to assist the nasotracheal tube passing the nasal cavity, nasopharynx, oropharynx and advanced into the trachea

Detailed description

In oro-maxillo-facial surgery, it is a common practice for patients receiving general anesthesia with nasotracheal intubation to widen the surgical field and to ease undergoing surgery. However, a nasotracheal tube blindly passing through the nasal cavity may easily result in nasal cavity and oropharynx damages. In addition, the advancement of the tube from oropharynx into trachea may assist by either using magic forceps or cuff inflation technique. The aim of the study is to investigate either use a bougie or nasogastric tube to assist the nasotracheal tube passing the nasal cavity, nasopharynx, oropharynx, and advanced into the trachea. Patients were randomized into three groups by using either bougie or nasogastric tube to facilitate nasotracheal tube sliding through into trachea from assigned nostril and compared with the control group with a conventional technique. Hemodynamic changes in each time interval, each time taken of tube going through the nasal cavity, tube advanced from oropharynx into trachea were recorded. The incidence of using Magill Forceps to accurately place tube tip into trachea, intubation related side effects and complications were recorded at postoperative time stages.

Interventions

DEVICEbougie

The endotracheal tube is used in the bougie mode under the direct view of the electronic imaging laryngoscope.

DEVICENasogastric(NG) tube

The endotracheal tube is used in the NG tube mode under the direct view of the electronic imaging laryngoscope.

Sponsors

Kaohsiung Medical University Chung-Ho Memorial Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Intervention model description

bougie or nasogastric tube

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Age:20-65 years * Undergoing oro-maxillofacial surgery * Opening mouth \> 3 cm * Denied any systemic disease. * American Society of Anesthesiologists (ASA) class:I-III

Exclusion criteria

* Difficult airway assessed (limited mouth opening, limited neck motion, and thyromental distance \< 6cm) * Previous head and neck surgery history * Upper abnormal airway diagnosed * Easily epistaxis * Both sides nasal cavities obstruction

Design outcomes

Primary

MeasureTime frameDescription
success rate of tube advancement and successful first tube attempt10 minutessuccess rate of tube passing through nasal cavity into trachea
time taken in tube advancement10 minutestime taken in tube advancement from nostril into trachea in each time interval

Secondary

MeasureTime frameDescription
post-intubation induced hoarseness and sore throat2 daysA visiting questionnaire is used to measure the condition of post-intubation, including sore throat, hoarseness, dysphagia, nasal occlusion, nosebleed and nasal pain. The score for the measurement of sore throat, hoarseness, dysphagia is divided into four degrees: none, mild, moderate and severe; on the other hand, The score for the measurement of nasal occlusion, nosebleed and nasal pain is divided into yes or no. All the evaluation will be assessed in the next coming morning after the postoperation.

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026