Ignite Creation Date:
2024-10-25 @ 7:53 PM
Last Modification Date:
2024-10-26 @ 3:41 PM
Study NCT ID:
NCT06618625
Status:
NOT_YET_RECRUITING
Last Update Posted:
None
First Post:
2024-09-26
Brief Title:
Tube Rotation for Tube Passage Into the Oral Cavity in Nasotracheal Intubation
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effect of Tube Rotation on Passage of Tracheal Tube Through Nasopharynx Into the Oral Cavity in 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 tube rotation on passage of the tracheal tube through the nasopharynx into the oral cavity in nasotracheal intubation
Detailed Description:
This prospective randomized controlled study was approved by IRB of our institute
Patients requiring nasotracheal intubation will be screened for eligibility of the study Then patients will be randomized to one of two groups group I tube advancement in neutral group II tube advancement with the tube counter-clockwise rotated After induction of anesthesia and muscle relaxation the preformed nasal RAE Ring-Adair-Elwyn tube will be inserted via a nostril approximately 3-4 cm Next an anesthesiologist will advance the tube with it neutral continuously into the oral cavity of the patients in Group I while the anesthesiologist will advance the tube with it rotated counter-clockwise in 90 degree into the oral cavity of the patients in Group II After the tube will be placed in the oral cavity the anesthesiologist will perform nasotracheal intubation with Magill forceps After that an investigator will check occurrence of epistaxis due to nasotracheal intubation and its severity with a fiberoptic bronchoscope After obtainment of all data investigators will analyze incidence of epistaxis and its severity between two groups
Patients requiring nasotracheal intubation will be screened for eligibility of the study Then patients will be randomized to one of two groups group I tube advancement in neutral group II tube advancement with the tube counter-clockwise rotated After induction of anesthesia and muscle relaxation the preformed nasal RAE Ring-Adair-Elwyn tube will be inserted via a nostril approximately 3-4 cm Next an anesthesiologist will advance the tube with it neutral continuously into the oral cavity of the patients in Group I while the anesthesiologist will advance the tube with it rotated counter-clockwise in 90 degree into the oral cavity of the patients in Group II After the tube will be placed in the oral cavity the anesthesiologist will perform nasotracheal intubation with Magill forceps After that an investigator will check occurrence of epistaxis due to nasotracheal intubation and its severity with a fiberoptic bronchoscope After obtainment of all data investigators will analyze incidence of epistaxis and its severity between 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