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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03226002
Date of registration: 18/07/2017
Prospective Registration: No
Primary sponsor: Kocaeli University
Public title: Which Nostril Should be Used for Nasotracheal Intubation With Airtraq NT®: the Right or Left? A Randomized Clinical Trial
Scientific title: Which Nostril Should be Used for Nasotracheal Intubation With Airtraq NT®: the Right or Left? A Randomized Clinical Trial
Date of first enrolment: April 1, 2017
Target sample size: 35
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT03226002
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Diagnostic. Masking: Double (Participant, Outcomes Assessor).  
Phase:  N/A
Countries of recruitment
Turkey
Contacts
Name:     zehra I Arslan
Address: 
Telephone:
Email:
Affiliation:  Anesthesiology and Reanimation
Key inclusion & exclusion criteria

Inclusion Criteria:

- 18-65 years of age

- undergoing elective maxillofacial surgery

- dental surgery

- plastic surgery requiring nasotracheal intubation

- ASA I-II

Exclusion Criteria:

- >18 years and > 65 years

- BMI> 35

- ASA III-IV

- fasted patients

- patients do not require nasotracheal intubation



Age minimum: 18 Years
Age maximum: 65 Years
Gender: All
Health Condition(s) or Problem(s) studied
Nasotracheal Intubation
Intervention(s)
Device: Airtraq NT
Primary Outcome(s)
insertion time of the device [Time Frame: 20 seconds]
nasotracheal intubation time with the device [Time Frame: 30 seconds]
total nasotracheal intubation time with the device [Time Frame: 40 seconds]
Secondary Outcome(s)
minor complications related to the device [Time Frame: 40 seconds]
optimisation maneuvers during intubation with the device [Time Frame: 20 seconds]
Secondary ID(s)
KÜ GOKAEK 2017/71
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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