Status:
WITHDRAWN
Effect of Gum Chewing on Sore Throat After Double-lumen Tube Intubation
Lead Sponsor:
Seoul National University Hospital
Conditions:
Thoracic Surgery, Video-Assisted
Chewing Gum
Eligibility:
All Genders
19-75 years
Phase:
NA
Brief Summary
Patients undergoing video-assisted thoracoscopic surgery requiring double-lumen tube intubation are randomized into two groups; gum group and control group. In the gum group, patients are instructed t...
Detailed Description
Patients scheduled for video-assisted thoracoscopic surgery requiring double-lumen tube intubation and who agree to participate in the study are randomized to the gum chewing group and the control gro...
Eligibility Criteria
Inclusion
- Patients aged 19-75 years undergoing routine video-assisted thoracoscopic surgery scheduled for double-lumen tube intubation
- Patients who are able to provide written informed consent to participate in the study and understand the procedures of this study
- American Society of Anesthesiologists physical status classification (ASA physical status classification) grade 1-2
Exclusion
- Patients who have not consented to the study
- American Society of Anesthesiologists physical status classification (ASA physical status classification) grade 3-4
- Patients with poor dental health that limits chewing gum or tracheal intubation
- Patients who are expected to be difficult to intubate
- Patients with a history of aspiration pneumonia
- Patients being treated for chronic laryngitis, chronic bronchitis, asthma, reflux esophagitis
- Patients with a history of smoking within the past week
- Patients who have difficulty communicating or carrying out gum chewing and spitting instructions
- Patients with hypersensitivity to Xylitol gum ingredients
- Patients taking narcotic analgesics, antidepressants, and anticonvulsants for chronic pain
- Patients requiring endotracheal intubation or intensive care unit treatment after surgery
- Patients who, in the opinion of the investigator or study staff, are not appropriate candidates for this study
Key Trial Info
Start Date :
October 24 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 31 2024
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT06061250
Start Date
October 24 2023
End Date
October 31 2024
Last Update
May 18 2025
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.