Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Two Handed Jaw-thrust on Postoperative Sore Throat After Double-lumen Endotracheal Tube Insertion

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03331809
Recruitment Status : Completed
First Posted : November 6, 2017
Last Update Posted : March 18, 2019
Sponsor:
Information provided by (Responsible Party):
Keimyung University Dongsan Medical Center

Brief Summary:
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 double-lumen endotracheal intubation.

Condition or disease Intervention/treatment Phase
Lung Surgery Procedure: Two-handed jaw thrust Procedure: Conventional intubation Not Applicable

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 106 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: Influence of Two-handed Jaw Thrust on Postoperative Sore Throat in Patients Undergoing Double-lumen Endobronchial Tube Insertion
Actual Study Start Date : December 11, 2017
Actual Primary Completion Date : May 1, 2018
Actual Study Completion Date : May 2, 2018

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Sore Throat

Arm Intervention/treatment
Active Comparator: Control Procedure: Conventional intubation
The attending anesthesiologist provided intubation with double-lumen tube endotracheal tube without two-handed jaw thrust.

Experimental: Two-hand Procedure: Two-handed jaw thrust
The assistant applied two-handed jaw thrust when intubating with double-lumen tube endotracheal tube.




Primary Outcome Measures :
  1. Number of participants with postoperative sore throat for postoperative 24 h [ Time Frame: At 24 hr ]

Secondary Outcome Measures :
  1. Number of participants with postoperative sore throat [ Time Frame: At 1, 6, and 24 hr ]
  2. Postoperative sore throat scores [ Time Frame: At 1, 6, and 24 hr ]
    Visual anlogue scales will be used (10: most imaginable pain, 0: no pain).

  3. Number of participants with postoperative hoarseness [ Time Frame: At 1, 6, and 24 hr ]
  4. Number of participants with postoperative shivering [ Time Frame: At 1, 6, and 24 hr ]
  5. Wound pain scores [ Time Frame: At 1, 6, and 24 hr ]
    Visual anlogue scales will be used (10: most imaginable pain, 0: no pain).

  6. Jaw discomfort scores [ Time Frame: At 1, 6, and 24 hr ]
    Visual anlogue scales will be used (10: most imaginable pain, 0: no pain).



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years to 80 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • ASA I-III
  • Patients scheduled for double-lumen endotracheal intubation

Exclusion Criteria:

  • Difficult airway
  • Mallampatti scores greater than 3
  • Recent sore throat
  • Cervical spine disease
  • History of head and neck surgery

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03331809


Locations
Layout table for location information
Korea, Republic of
Keimyung University
Daegu, Non-US/Canada, Korea, Republic of, 137-040
Sponsors and Collaborators
Keimyung University Dongsan Medical Center
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Layout table for additonal information
Responsible Party: Keimyung University Dongsan Medical Center
ClinicalTrials.gov Identifier: NCT03331809    
Other Study ID Numbers: 2017-11-002
First Posted: November 6, 2017    Key Record Dates
Last Update Posted: March 18, 2019
Last Verified: June 2018

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Keimyung University Dongsan Medical Center:
intubation
pharyngitis
Additional relevant MeSH terms:
Layout table for MeSH terms
Pharyngitis
Pharyngeal Diseases
Stomatognathic Diseases
Respiratory Tract Infections
Respiratory Tract Diseases
Otorhinolaryngologic Diseases