Anesthesia, General Clinical Trial
Official title:
The Clarus Video System (Trachway) and Direct Laryngoscope for Endotracheal Intubation With Cricoid Pressure in Simulated Rapid Sequence Induction Intubation: A Prospective Randomized Controlled Trial
Verified date | November 2016 |
Source | Chang Gung Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
During an emergency endotracheal intubation, rapid sequence induction intubation with cricoid pressure is frequently implemented to prevent aspiration pneumonia. When properly applied, cricoid pressure may not affect glottic view during endotracheal intubation with either a direct laryngoscope or a video laryngoscope. However, the application of cricoid pressure is likely to prolong the intubation time. Limited mouth opening or vulnerable teeth, which often accompany the patients requiring emergency intubation, are the two common factors to deter the intubators from using a laryngoscopic device. Besides, the blade of a laryngoscopic device is often too bulky for a narrow mouth opening, and the blade always bears a level force on upper incisors while the intubator is lifting epiglottis during intubation, which is liable to tooth fracture. In this prospective randomized study, the investigators compare the use of the Clarus Video System and that of direct laryngoscope (Macintosh Laryngoscope) in patients undergoing endotracheal intubation in simulated rapid sequence induction intubation for the primary goals of the first attempt success rate and intubation time.
Status | Completed |
Enrollment | 150 |
Est. completion date | April 14, 2018 |
Est. primary completion date | April 13, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years and older |
Eligibility |
Inclusion Criteria: - Older than 20 years of age - Scheduled for elective surgery under general anesthesia Exclusion Criteria: - BMI (Body Mass Index) > 35 kg/m2 - Interincisor distance < 3 cm - Poor dentition - Upper airway tumor - Limited neck mobility - Pregnancy - History of difficult tracheal intubation |
Country | Name | City | State |
---|---|---|---|
Taiwan | Chang Gung Memorial Hospital | Taoyuan |
Lead Sponsor | Collaborator |
---|---|
Chang Gung Memorial Hospital |
Taiwan,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The first attempt success rate | After intubation immediately | ||
Primary | Intubation time | Intubation time was counted from the inserting the device into the patient's mouth to viewing the endotracheal tube into the trachea. | After intubation immediately | |
Secondary | Blood pressure | Measure blood pressure in millimeter of mercury by non-invasive blood pressure before induction, 1 minute after intubation, and 5 minutes after intubation | 1 minute and 5 minutes after intubation | |
Secondary | Heart rate | Measure heart rate in beats per minute by electrocardiography monitor before induction, 1 minute after intubation, and 5 minutes after intubation | 1 minute and 5 minutes after intubation | |
Secondary | Sore throat | Documented by a blinded observer on the next day. Sore throat was graded according to numerical rating scale (NRS): none, NRS = 0; mild, NRS = 1-3; moderate, NRS = 4-6; severe, NRS = 7-10. | On postoperative day 1 | |
Secondary | Mucosal injury | Documented by a blinded observer on the next day. "Yes" is defined as any oral mucosal lesion reported by participants. | On postoperative day 1 |
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