Clinical Trials Directory

Trials / Completed

CompletedNCT04857190

Parker Flex-it Stylet Versus Malleable Stylet in Orotracheal Intubation Using a Fiber-optic Laryngoscope

Parker Flex-it Directional Stylet Versus Conventional Malleable Stylet in Elective Orotracheal Intubation Using a Fiber-optic Laryngoscope

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Damanhour Teaching Hospital · Other Government
Sex
All
Age
21 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Objectives: To compare the safety and efficacy of Parker flex-it directional stylet (PFDS) versus conventional malleable stylet (CMS) in orotracheal intubation (OTI) using fiber-optic Macintosh laryngoscope. Background: OTI is used in general anesthesia for anesthetic delivery and ventilation of patients. OTI delay or failure may adversely affect patient outcomes, therefore, anesthetists with sufficient clinical experience and skill should perform OTI. However, in emergency situations, experienced anesthetists may not be available, and the patient may have a high Cormack-Lehane grade. A stylet is commonly used in the emergency department to aid insertion of the endotracheal tube during direct laryngoscopy. Patients and Methods: This was a prospective, randomized, double-blind clinical trial; carried out on 80 patients requiring OTI under general anesthesia at our hospital. Patients were randomly allocated into two equal groups; group DS, intubated using PFDS, and group MS, intubated using CMS.

Conditions

Interventions

TypeNameDescription
DEVICEParker Flex-it Directional StyletParker Flex-it Directional Stylet
DEVICEConventional Malleable StyletConventional Malleable Stylet

Timeline

Start date
2021-05-01
Primary completion
2022-03-15
Completion
2022-03-15
First posted
2021-04-23
Last updated
2022-04-22

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04857190. Inclusion in this directory is not an endorsement.