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NCT00908817 Clinical Trial

Triamcinolone Paste to Reduce the Incidence of Postoperative Sore Throat

Tracheal Intubation Clinical Trial

Official title:
Triamcinolone Paste to Reduce the Incidence of Postoperative Sore Throat

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00908817
Other study ID # ST
Secondary ID
Status Completed
Phase N/A
First received May 21, 2009
Last updated May 26, 2009
Start date May 2008
Est. completion date May 2009

Study information
Verified date May 2009
Source Soonchunhyang University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether triamcinolone paste applied over tracheal tube is effective to reduce the incidence of postoperative sore throat after tracheal intubation.

Description:

Sore throat is a common postoperative complaint after tracheal intubation. When the surgical pain is well controlled, sore throat is often the predominant complaint, therefore it is important to prevent sore throat.

Recruitment information / eligibility
Status Completed
Enrollment 150
Est. completion date May 2009
Est. primary completion date April 2009
Accepts healthy volunteers
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- ASA physical status I-II, aged between 20 and 70 years

- scheduled for elective laparoscopic cholecystectomy under general anesthesia with endotracheal intubation

Exclusion Criteria:

- recent respiratory tract infection or sore throat

- who were using analgesics or steroid preoperatively

- who have risk factors for oral cavity infection

- the surgical duration < 60 minutes or > 300 minutes

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• triamcinolone acetonide
paste applied over tracheal tube for lubrication
• chlorhexidine gluconate
jelly applied over tracheal tube for lubrication

Locations
Country Name City State
Korea, Republic of Soonchunhyang University, College of medicine Bucheon Hospital 1174 Jung-Dong, Wonmi-Gu, Bucheon-Si Gyeonggi-Do

Sponsors (1)
Lead Sponsor Collaborator
Soonchunhyang University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary the incidence of postoperative sore throat postoperative day 1
Secondary the severity of postoperative sore throat postoperative day 1
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