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Completed

NCT Number: NCT06515808

Effects of Three Airway Instruments on the Incidence of Postoperative Sore Throat

Postoperative sore throat (POST) is a common complaint after general anesthesia. POST is defined by the presence of a self-reported foreign body sensation or a painful sensation in the throat after general anesthesia. This condition may affect recovery and patient satisfaction and is associated with many factors, including intubation tools. Previous studies have reported conflicting results on POST. This retrospective cohort study, with sample size of 10,382 patients, was conducted to confirm the hypothesis that the use of video laryngoscopy (VL) is associated with a lower incidence of POST compared with direct laryngoscopy (DL).

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Key information

Age range

20 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Fu Jen Catholic University Hospital

New Taipei City, 24300, Taiwan

About this study

Background: Postoperative sore throat (POST) is a common complaint after general anesthesia. POST is defined by the presence of a self-reported foreign body sensation or a painful sensation in the throat after general anesthesia. This condition may affect recovery and patient satisfaction and is associated with many factors, including intubation tools. Previous studies have reported conflicting results on POST. This retrospective cohort study, with sample size of 10,382 patients, was conducted to confirm the hypothesis that the use of video laryngoscopy (VL) is associated with a lower incidence of POST compared with direct laryngoscopy (DL).

Methods: Data were extracted from a prospectively maintained quality improvement database. A total of 10,382 patients were included in the study. Statistical analysis was conducted for comparisons of demographic characteristics and to determine the effect of intubation tools on the incidence of POST.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients receiving inpatients surgery and general anesthesia with tracheal intubation

Exclusion criteria

  • Having difficult airway,
  • Anticipated difficult airway:
  • Abnormal cervical spine movement or temporomandibular joint movement
  • Airway-compromising masses such as tumors, cysts, or hematomas
  • A Mallampati score greater than 3
  • A thyromental distance of less than 6 cm
  • A lesion below vocal cord
  • A previously identified difficult airway
  • Unexpected difficult airway
  • difficult mask ventilation
  • difficult vocal cord visualization after multiple attempts of laryngoscopy
  • Receiving laryngeal surgery, such as laryngeal biopsy, laryngeal microsurgery, laryngoplasty or vocal cord surgery,
  • Not being extubated at the end of anesthesia,
  • Being pregnant,
  • Being under 20 years of age,
  • American Society of Anesthesiologists (ASA) physical status class greater than 3.

Treatment and study plan

Direct Laryngoscope

Device

Patient receiving tracheal intubation with direct laryngoscope, GlideScope or Airway Scope

Other names: GlideScope AVL, AirwayScope S100

Primary outcomes

  1. Postoperative sore throat (POST)

    Time frame: 12 to 24 hours after general anesthesia is finished

    POST is defined by the presence of a self-reported foreign body sensation or a painful sensation in the throat after general anesthesia.

Sponsors and collaborators

Lead sponsor

Fu Jen Catholic University Hospital

Other

Registry information

Official study title

Effects of GlideScope, Pentax Airway Scope, and Macintosh Blade on the Incidence of Postoperative Sore Throat: A Cohort Study of 10,382 Patients

Important dates

Study start
2018
Primary completion
2022
Study completion
2022
First posted
Jul 23, 2024
Registry last updated
Jul 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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