Two Handed Jaw-thrust on Postoperative Sore Throat After Double-lumen Endotracheal Tube Insertion

Lung Surgery Clinical Trial

Official title:

Influence of Two-handed Jaw Thrust on Postoperative Sore Throat in Patients Undergoing Double-lumen Endobronchial Tube Insertion

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03331809
• Other study ID #: 2017-11-002
• Status: Completed
• Phase: N/A
• 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
• 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

Related Conditions & MeSH terms

• Lung Surgery
• Pharyngitis

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