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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03693417
Other study ID # HeatPOSTSingle
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date November 1, 2019

Study information

Verified date October 2018
Source Keimyung University Dongsan Medical Center
Contact Hyun-Chang Kim
Phone +821028862876
Email onidori1979@gmail.com
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 heated breathing circuit in patients undergoing endotracheal intubation for general anesthesia.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 92
Est. completion date November 1, 2019
Est. primary completion date November 1, 2019
Accepts healthy volunteers No
Gender All
Age group 19 Years to 80 Years
Eligibility Inclusion Criteria:

- ASA I-III

- Patients scheduled for general anesthesia with 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Keimyung University Dongsan Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary Number of participants with postoperative sore throat for postoperative 24 hour At 24 hour
Secondary Number of participants with postoperative sore throat At 2, 4, and 24 hour
Secondary Number of participants with postoperative hoarseness At 2, 4, and 24 hour
Secondary Wound pain scores Visual analogue scales will be used (10: most imaginable pain, 0: no pain). At 2, 4, and 24 hour
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