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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