Viewing Study NCT06515808



Ignite Creation Date: 2024-10-25 @ 8:01 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06515808
Status: COMPLETED
Last Update Posted: None
First Post: 2024-07-14

Brief Title: Effects of Three Airway Instruments on the Incidence of Postoperative Sore Throat
Sponsor: None
Organization: None

Study Overview

Official Title: Effects of GlideScope Pentax Airway Scope and Macintosh Blade on the Incidence of Postoperative Sore Throat A Cohort Study of 10382 Patients
Status: COMPLETED
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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 10382 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
Detailed Description: 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 10382 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 10382 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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None