Viewing Study NCT06605989



Ignite Creation Date: 2024-10-26 @ 3:40 PM
Last Modification Date: 2024-10-26 @ 3:40 PM
Study NCT ID: NCT06605989
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-09-18

Brief Title: Nostril Side on Epistaxis
Sponsor: None
Organization: None

Study Overview

Official Title: The Effect of Nostril Side on Epistaxis During Nasotracheal Intubation
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-09
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: The purpose of the study is to investigate the effect of the nostril side on epistaxis during nasotracheal intubation
Detailed Description: This prospective randomized controlled study was approved by the IRB of our institute

Patients requiring nasotracheal intubation will be screened for eligibility for the study Then patients will be randomized to one of two groups Group I tube will be inserted through the left nostril and advanced into the oral cavity Group II tube will be inserted through the right nostril and advanced into the oral cavity After induction of anesthesia and muscle relaxation the preformed nasal RAE Ring-Adair-Elwyn tube will be inserted via the nostril which is assigned to each patient according to the group approximately 3-4 cm Next an anesthesiologist will advance the tube into the oral cavity After the tube is placed in the oral cavity the anesthesiologist will perform nasotracheal intubation with Magill forceps After that an investigator will check the occurrence of epistaxis due to nasotracheal intubation and its severity with a fiberoptic bronchoscope After obtaining all data investigators will analyze the incidence of epistaxis and its severity between the two groups

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