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Effect on Postoperative Sore Throat of Lidocaine Jelly Application Over the Endotracheal Tube of Tapered-shaped Cuff

NCT ID: NCT02952157

Last Updated: 2016-11-02

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

UNKNOWN

Clinical Phase

PHASE4

Total Enrollment

210 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-11-30

Study Completion Date

2016-11-30

Brief Summary

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Postoperative sore throat is a complication after general anesthesia requiring endotracheal intubation. The investigators will evaluate the efficacy of lidocaine jelly application on the endotracheal tube with taper-shaped cuff regarding postoperative sore throat.

Detailed Description

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Conditions

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Sore Throat

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Control

Normal saline will be applied to the endotracheal tube.

Group Type SHAM_COMPARATOR

Normal saline application

Intervention Type DRUG

Lidocaine

Lidocaine jelly will be applied to the endotracheal tube.

Group Type ACTIVE_COMPARATOR

Lidocaine jelly application

Intervention Type DRUG

Interventions

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Lidocaine jelly application

Intervention Type DRUG

Normal saline application

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* ASA I-III
* Patients scheduled for general anesthesia with endotracheal intubation
* Patients scheduled for surgery which duration is expected to less than 3 hr

Exclusion Criteria

* Difficult airway
* Rapid sequence induction
* Recent sore throat
* Recent upper respiratory infection
* Asthma
* Chronic obstructive pulmonary disease
* Chronic cough
* Pregnancy
* Allergy to lidocaine
* Friable teeth
* History of head and neck surgery
* Multiple intubation attempts
* Regional anesthetic agents
* Gastric tube
* Dexamethasone
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Keimyung University Dongsan Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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LidoTaper

Identifier Type: -

Identifier Source: org_study_id