Triamcinolone Paste to Reduce the Incidence of Postoperative Sore Throat

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

150 participants

Study Classification

INTERVENTIONAL

Study Start Date

2008-05-31

Study Completion Date

2009-05-31

Brief Summary

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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.

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Detailed Description

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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.

Conditions

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Tracheal Intubation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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triamcinolone

Group Type ACTIVE_COMPARATOR

triamcinolone acetonide

Intervention Type DRUG

paste applied over tracheal tube for lubrication

chlorhexidine

Group Type PLACEBO_COMPARATOR

chlorhexidine gluconate

Intervention Type DRUG

jelly applied over tracheal tube for lubrication

Interventions

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triamcinolone acetonide

paste applied over tracheal tube for lubrication

Intervention Type DRUG

chlorhexidine gluconate

jelly applied over tracheal tube for lubrication

Intervention Type DRUG

Eligibility Criteria

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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

Minimum Eligible Age

20 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No