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The Effect of Reinforced Endotracheal Tube on Post-operative Hoarseness Undergoing Thyroidectomy

C

Chonnam National University

Status

Completed

Conditions

Voice Hoarseness
Sore Throat
Thyroidectomy

Treatments

Device: Oral/Nasal Endotracheal Tube, Reinforced (Covidien)
Device: TaperGuard oral tracheal tube (Covidien)

Study type

Interventional

Funder types

Other

Identifiers

NCT03368911
CNUHH-2017-102

Details and patient eligibility

About

The purpose of this study is an evaluation of the effect of the reinforced endotracheal tube on post-operative hoarseness and sore throat undergoing thyroidectomy

Enrollment

140 patients

Sex

All

Ages

20 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American Society of Anesthesiologist physical status 1-3
  • Patients undergoing thyroidectomy under general anesthesia
  • Tumor size < 2cm
  • Patient who do not have any problem in the vocal cord

Exclusion criteria

  • Patient who is expected difficult intubation (Mallampati class 3 or more)
  • Patient who has respiratory disorder
  • Previous hoarseness and sore throat history
  • Obesity (BMI > 30 kg/m2)
  • Recurrent laryngeal injury during operation
  • Operation history of oral and laryngeal surgery

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

140 participants in 2 patient groups

Reinforced tube group
Experimental group
Description:
use an reinforced endotracheal tube for endotracheal intubation during general anesthesia undergoing thyroidectomy
Treatment:
Device: Oral/Nasal Endotracheal Tube, Reinforced (Covidien)
Conventional tube group
Active Comparator group
Description:
use an conventional endotracheal tube for endotracheal intubation during general anesthesia undergoing thyroidectomy
Treatment:
Device: TaperGuard oral tracheal tube (Covidien)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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