asal Intubatio
Phase 2
- Conditions
- asotracheal Intubation.
- Registration Number
- IRCT201309247604N1
- Lead Sponsor
- Vice chancellor for research, Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 160
Inclusion Criteria
patients undergo maxillofacial surgeries who need nasotracheal intubation; age between 15 to 65; ASA class I and II.
Exclusion criteria: patient younger than 15-year-old; patients with difficult or compromised airway; patients who have restrictions in mouth opening; coagulopathy; patients who don't have neurosurgery permission for nasal intubation; cases who need size 6 of tracheal tube or less; emergency or non-elective surgery.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method eed to use Magill Forceps. Timepoint: During intubation, After intervention. Method of measurement: using or not using Magill During intubation.;Effects of using Bougie in reducing numbers of attempts to nasal intubation. Timepoint: After Intubation. Method of measurement: Count the number of trials.
- Secondary Outcome Measures
Name Time Method Bleeding. Timepoint: During intubation, After intervention. Method of measurement: Observation and confirmation of anesthesiologist.;Need to use Direct Laryngoscopy via Machintosh Laryngoscope. Timepoint: During intubation, After intervention. Method of measurement: Use of Machintosh Laryngoscope for intubation.;Trauma to soft tissue of mouth and soft palate. Timepoint: During intubation, After intervention. Method of measurement: Observation and confirmation of anesthesiologist.;Total time of intubation. Timepoint: From begining to the end of intubation process. Method of measurement: chornometer.