Heated Breathing Circuit on Postoperative Sore Throat After Double-lumen Endobronchial Tube Insertion

Lung Surgery Clinical Trial

Official title:

Influence of Heated Breathing Circuit on Postoperative Sore Throat in Patients Undergoing Double-lumen Endobronchial Tube Insertion

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03689127
• Other study ID #: Heated Circuit POST
• Status: Not yet recruiting
• Phase: N/A
• Start date: November 2018
• Est. completion date: November 2019

Study information

• Verified date: September 2018
• Source: Keimyung University Dongsan Medical Center
• Contact: Hyun Chang Kim
• Phone: +821028862876
• Email: onidori1979[@]gmail.com
• 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 heated breathing circuit in patients undergoing double-lumen endotracheal intubation.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 106
• Est. completion date: November 2019
• Est. primary completion date: November 2019
• 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 2

• Recent sore throat

• Cervical spine disease

• Recent upper respiratory infection

• Recent analgesics

• History of head and neck surgery

• Friable teeth

• Multiple intubation attempts

Related Conditions & MeSH terms

• Lung Surgery
• Pharyngitis

Intervention

Device:
• Heated breathing circuit on
Heated breathing circuit will be turned on.
• Heated breathing circuit off
Heated breathing circuit will be turned off.

Locations

Country	Name	City	State
Korea, Republic of	Hyun-Chang Kim	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 hours
Secondary	Number of participants with postoperative sore throat		At 1, 6, and 24 hours
Secondary	Postoperative sore throat scores		At 1, 6, and 24 hours
Secondary	Number of participants with postoperative hoarseness		At 1, 6, and 24 hours
Secondary	Number of participants with postoperative shivering		At 1, 6, and 24 hours
Secondary	Wound pain scores	Visual anlogue scales will be used (10: most imaginable pain, 0: no pain).	At 1, 6, and 24 hours
Secondary	Jaw discomfort scores	Visual anlogue scales will be used (10: most imaginable pain, 0: no pain).	At 1, 6, and 24 hours