Ignite Creation Date:
2024-05-06 @ 8:20 PM
Last Modification Date:
2024-10-26 @ 3:25 PM
Study NCT ID:
NCT06349005
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-04-05
First Post:
2024-02-26
Brief Title:
Laryngoscopy and Coronary Artery Bypass Graft Surgery
Sponsor:
Konya Meram State Hospital
Organization:
Konya Meram State Hospital
Study Overview
Official Title:
Hemodynamic Response to Various Laryngoscopes During Tracheal Intubation in CABG Patients
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-03
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:
VL
Brief Summary:
In this prospective randomized controlled trial the purpose is to compare Macintosh laryngoscope EzVision video laryngoscope McGrath video laryngoscope and Storz video laryngoscope in terms of hemodynamic response associated with intubation in adult patients undergoing Coronary Artery Bypass Surgery CABG
Detailed Description:
During endotracheal intubation laryngoscopy can significantly affect hemodynamic responses including tachycardia and elevated blood pressure which may be particularly detrimental to individuals with cardiovascular conditions Various studies have explored the hemodynamic reactions associated with laryngeal stimulation through different intubation devices Researchers hypothesize that endotracheal intubation using video laryngoscopy will elicit a reduced hemodynamic response compared to traditional Macintosh laryngoscopy In this prospective and randomized clinical study the purpose is to compare the Macintosh laryngoscope EzVision video laryngoscope McGrath video laryngoscope and Storz video laryngoscope concerning haemodynamic response associated with intubation in adult patients undergoing Coronary Artery Bypass Surgery CABG
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