Viewing Study NCT06436196



Ignite Creation Date: 2024-06-16 @ 11:48 AM
Last Modification Date: 2024-10-26 @ 3:30 PM
Study NCT ID: NCT06436196
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-05-31
First Post: 2024-05-19

Brief Title: Video Laryngoscopy vs Direct Laryngoscopy in Paediatric Patients
Sponsor: Watim Medical Dental College
Organization: Watim Medical Dental College

Study Overview

Official Title: Video Laryngoscopy Versus Direct Laryngoscopy for Elective Airway Management in Pediatrics Anesthesia Comparison of Out-comes
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this interventional study is to compare the effectiveness of direct laryngoscopy vs video laryngoscopy in paediatric population aged 2 to 8 years presenting for elective surgeries having uncomplicated airways

The primary outcome measures include

1 Time taken for succesful insertion and confirmation of ETT in patients using both techniques seprately
2 Rate of complications and failed attempts compared between both modalities
Detailed Description: The comparision of efficacy of Video Laryngoscopy for pediatric airway vs Direct Laryngoscopy is the goal of this study Safety of the patients will be the utmost priority with careful case selection alongwith proper informed detailed consent from the guardians of the children

PROCEDURE

After induction of General Anesthesia four minutes of proper bag mask ventilation to allow for proper intubating conditions will be done The time taken from the insertion of the laryngoscopic blade to the best glottic view acheived by the specific technique will be noted seperately and then the time to the succesful acheivement of lung inflation with the proper placement of ETT will be noted seperately both of these parameters will be recorded

If in a patient airway is not secured even after 3 attempts by a specific technique the technique would be altered and patient would be excluded from our research

MATERIALS

Randomized allotment of patients into the 2 groups ie Direct Laryngoscopy and Video Laryngoscopy would be done

Study Oversight

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