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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03331809
Other study ID # 2017-11-002
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 11, 2017
Est. completion date May 2, 2018

Study information

Verified date June 2018
Source Keimyung University Dongsan Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This investigation is planned to compare the incidence and severity of postoperative sore throat according to the use of two-handed jaw thrust maneuver in patients undergoing double-lumen endotracheal intubation.


Recruitment information / eligibility

Status Completed
Enrollment 106
Est. completion date May 2, 2018
Est. primary completion date May 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- ASA I-III

- Patients scheduled for double-lumen endotracheal intubation

Exclusion Criteria:

- Difficult airway

- Mallampatti scores greater than 3

- Recent sore throat

- Cervical spine disease

- History of head and neck surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Two-handed jaw thrust
The assistant applied two-handed jaw thrust when intubating with double-lumen tube endotracheal tube.
Conventional intubation
The attending anesthesiologist provided intubation with double-lumen tube endotracheal tube without two-handed jaw thrust.

Locations

Country Name City State
Korea, Republic of Keimyung University Daegu Non-US/Canada

Sponsors (1)

Lead Sponsor Collaborator
Keimyung University Dongsan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with postoperative sore throat for postoperative 24 h At 24 hr
Secondary Number of participants with postoperative sore throat At 1, 6, and 24 hr
Secondary Postoperative sore throat scores Visual anlogue scales will be used (10: most imaginable pain, 0: no pain). At 1, 6, and 24 hr
Secondary Number of participants with postoperative hoarseness At 1, 6, and 24 hr
Secondary Number of participants with postoperative shivering At 1, 6, and 24 hr
Secondary Wound pain scores Visual anlogue scales will be used (10: most imaginable pain, 0: no pain). At 1, 6, and 24 hr
Secondary Jaw discomfort scores Visual anlogue scales will be used (10: most imaginable pain, 0: no pain). At 1, 6, and 24 hr
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