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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02876913
Other study ID # 4-2016-0504
Secondary ID
Status Completed
Phase N/A
First received August 16, 2016
Last updated September 4, 2017
Start date August 24, 2016
Est. completion date June 23, 2017

Study information

Verified date September 2017
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The nasotracheal intubation is preferred for oral surgery; it provides an easier view of the surgical field. However, nasotracheal tubes are produced by foreign countries. Tubes are often not fitted in anatomy of Korean people because of small nostril. When the size of the tube is chosen by nostril size, the length of nasotracheal tube is not appropriate to the glottis. The aim of this study is to evaluate on the proper size of the nasotracheal tube and depth in nasotracheal intubation in Korean. Forty patients (20 males and 20 females) who are scheduled for nasal intubation for general anesthesia will be enrolled. The primary outcome is the proportion of patients who are in inappropriate insertion of nasotracheal tube; the proximal end of tube's cuff is less than 2 cm below vocal cord. The size of nostril, length from the nare to the carina and vocal cord are measured.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date June 23, 2017
Est. primary completion date June 23, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- Patients who are scheduled for nasotracheal intubation for general anesthesia

Exclusion Criteria:

- age < 20 years and age > 70 years

- ASA(American Society of Anesthesiologist) class III or more

- pregnancy

- emergency surgery

- nasal airway disease

- expected difficult intubation (difficult intubation history, Modified Mallampati score 4, mouth opening <2cm, facial anomaly)

- unstable teeth

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of the inappropriate insertion of nasotracheal tube the inappropriate insertion of nasotracheal tube; the proximal end of tube's cuff is less than 2 cm below vocal cord 5 minutes after induction of general anesthesia
See also
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