Jaw-thrust on Postoperative Sore Throat

September 27, 2018 updated by: Hyun-Chang Kim, Keimyung University Dongsan Medical Center

Influence of Two-handed Jaw Thrust on Postoperative Sore Throat

This investigation is planned to compare the incidence and severity of postoperative sore throat according to the use of two-handed jaw thrust maneuver in patients undergoing endotracheal intubation for general anesthesia.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Anticipated)

96

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
    • Non-US/Canada
      • Daegu, Non-US/Canada, Korea, Republic of, 137-040
        • Hyun-Chang Kim

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

19 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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 Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Control
The attending anesthesiologist provided intubation without two-handed jaw thrust.
Procedure: Control
The intubation was done without two-handed jaw thrust.
Experimental: Two-hand
The attending anesthesiologist provided intubation with two-handed jaw thrust.
Procedure: Two-handed jaw thrust
The assistant applied two-handed jaw thrust for intubation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of participants with postoperative sore throat for postoperative 24 hour
Time Frame: At postoperative 24 hour
At postoperative 24 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of participants with postoperative sore throat
Time Frame: At postoperative 2, 4, and 24 hour
At postoperative 2, 4, and 24 hour
Postoperative sore throat scores
Time Frame: At postoperative 2, 4, and 24 hour
Visual analogue scales will be used (10: most imaginable pain, 0: no pain).
At postoperative 2, 4, and 24 hour
Number of participants with postoperative hoarseness
Time Frame: At postoperative 2, 4, and 24 hour
At postoperative 2, 4, and 24 hour
Number of participants with postoperative shivering
Time Frame: At postoperative 2, 4, and 24 hour
At postoperative 2, 4, and 24 hour
Wound pain scores
Time Frame: At postoperative 2, 4, and 24 hour
Visual analogue scales will be used (10: most imaginable pain, 0: no pain).
At postoperative 2, 4, and 24 hour
Number of participants with jaw discomfort
Time Frame: At postoperative 2, 4, and 24 hour
At postoperative 2, 4, and 24 hour

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Keimyung University Dongsan Medical Center

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 1, 2018

Primary Completion (Anticipated)

July 1, 2019

Study Completion (Anticipated)

August 1, 2019

Study Registration Dates

First Submitted

June 4, 2018

First Submitted That Met QC Criteria

June 22, 2018

First Posted (Actual)

June 26, 2018

Study Record Updates

Last Update Posted (Actual)

September 28, 2018

Last Update Submitted That Met QC Criteria

September 27, 2018

Last Verified

September 1, 2018

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • JTPOST

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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