Sore Throat After Intubation Using Glidescope With Stylet and Bougie

Overview

This is a prospective double-blinded clinical trial aiming to compare the incidence and severity of sore throat after laparoscopic cholecystectomy when using two different techniques of intubation using glidescope

Full Title of Study: “Comparison Between Using Glidescope With Stylet Technique and With Bougie Technique on the Incidence and Severity of Postoperative Sore Throat Development”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: Randomized
    • Intervention Model: Crossover Assignment
    • Primary Purpose: Prevention
    • Masking: Triple (Participant, Care Provider, Investigator)
  • Study Primary Completion Date: March 30, 2020

Detailed Description

The first technique is loading the endotracheal tube on a stylet the second technique is sliding the endotracheal tube over a bogie that is dragged into the trachea at both techniques, the investigators are using glidescope

Interventions

  • Device: a device to facilitate endotracheal intubation
    • a device to facilitate endotracheal intubation

Arms, Groups and Cohorts

  • Active Comparator: stylet
    • The stylet is a device that is put inside the endotracheal tube to facilitate its insertion into the trachea
  • Active Comparator: bougie
    • The bougie is a device that is inserted into the trachea and an endotracheal tube is loaded over it and is slide into the trachea

Clinical Trial Outcome Measures

Primary Measures

  • postoperative sore throat (POST)
    • Time Frame: IMMEDIATELY POSTOPERATIVE AND 2 HORSE LATER
    • report severity of postoperative sore throat and CHANGES that could occur later on

Secondary Measures

  • postoperative sore throat (POST)
    • Time Frame: immediately postoperative at recovery room
    • INCIDENCE of postoperative sore throat

Participating in This Clinical Trial

Inclusion Criteria

  • ASA I, II UNDERGOING LAPAROSCOPIC CHOLECYSTECTOMY UNDER GA Exclusion Criteria:

  • ANTICIPATED DIFFICULT INTUBATION

Gender Eligibility: All

Minimum Age: 18 Years

Maximum Age: 50 Years

Are Healthy Volunteers Accepted: No

Investigator Details

  • Lead Sponsor
    • Suez Canal University
  • Provider of Information About this Clinical Study
    • Principal Investigator: Abdelrhman Alshawadfy, Lecturer of anesthesia and intensive care – Suez Canal University

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