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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:  NCT02625194
Date of registration: 25/11/2015
Prospective Registration: Yes
Primary sponsor: Yonsei University
Public title: The Utility of Oxygen Insufflation During Flexible Fiberoptic Bronchoscope-guided Intubation
Scientific title: The Utility of Oxygen Insufflation During Flexible Fiberoptic Bronchoscope-guided Intubation
Date of first enrolment: January 1, 2016
Target sample size: 36
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02625194
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Prevention. Masking: Single (Participant).  
Phase:  N/A
Countries of recruitment
Korea, Republic of
Contacts
Name:     Jeong Soo Lee, MD
Address: 
Telephone:
Email:
Affiliation:  Yonsei University Gangnam Severance Hospital
Key inclusion & exclusion criteria

Inclusion Criteria:

- patients who have surgery under general oral endotracheal anesthesia with invasive
arterial blood pressure monitoring

Exclusion Criteria:

- history of lung disease

- abnormality in chest x-ray

- anticipating difficult intubation

- pregnant women

- who is unable to understand and agree the consent form



Age minimum: 20 Years
Age maximum: 60 Years
Gender: All
Health Condition(s) or Problem(s) studied
Lumbar Spinal Stenosis
Intervention(s)
Drug: Oxygen
Primary Outcome(s)
Velocity of PaO2 decrease [Time Frame: from mask removal to 1st manual ventilation after intubation, up to 5 minute]
Secondary Outcome(s)
PaO2 [Time Frame: 1. 5 minutes after manual ventilation / 2.right before 1st manual ventilation after intubation, up to 5 minute]
visual field [Time Frame: throughout the intubation with bronchoscope, upto 5 minute]
success of intubation [Time Frame: 300 sec after the beginning of intubation]
PaCO2 [Time Frame: 1. 5 minutes after manual ventilation / 2.right before 1st manual ventilation after intubation, up to 5 minute]
pH [Time Frame: 1. 5 minutes after manual ventilation / 2.right before 1st manual ventilation after intubation, up to 5 minute]
Secondary ID(s)
3-2015-0218
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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