Ignite Creation Date:
2024-05-06 @ 3:07 PM
Last Modification Date:
2024-10-26 @ 1:43 PM
Study NCT ID:
NCT04520581
Status:
UNKNOWN
Last Update Posted:
2020-08-20
First Post:
2020-08-13
Brief Title:
The Use of O Shaped- Endotracheal Tube During Intubation for General Anesthesia Prospective Randomized Trial
Sponsor:
Seoul National University Hospital
Organization:
Seoul National University Hospital
Study Overview
Official Title:
The Use of O Shaped- Endotracheal Tube During Intubation for General Anesthesia Prospective Randomized Trial
Status:
UNKNOWN
Status Verified Date:
2020-08
Last Known Status:
RECRUITING
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:
This study is prospective randomized trial study O type tracheal intubation tube is anatomically consistent and will able to increase the success rate of first intubation without any other external help
Detailed Description:
This study is divided into two groups control vs O shape endotracheal tube
The investigator was studied 238 consecutive the American Society of Anesthesiologists physical grades I and II adult patients scheduled to undergo general anesthesia requiring tracheal intubation for elective surgery Exclusion criteria included a gross anatomical abnormality before surgery of the head neck and cervical spine previously difficult tracheal intubation loose teeth or those requiring a rapid sequence or awake intubation moderate or severe obstructiverestrictive pulmonary disease accompanied by pulmonary function tests Anesthesia was induced with remifentanyl 3ngkg propopol 1-2 mgkg or TIVA 2 fresopol 4ugdL remifentanyl 3ngdL and rocuronium 08 mgkg to facilitate tracheal intubation Laryngoscopy was performed after the loss of the fourth twitch in the train-of-four in response to ulnar nerve stimulation All laryngoscopies using a 4 Macintosh blade were performed with the patient placed in the sniffing position Tracheal intubation was performed without assistance ex External laryngeal manipulation Used stylet A single experienced anesthesiologist blinded to each group performed all of the direct laryngoscopies and classified the laryngoscopic view according to the modified Cormack and Lehane grade measured number of attempts intubation time and blood pressure and heart rate before after intubation
The investigator was studied 238 consecutive the American Society of Anesthesiologists physical grades I and II adult patients scheduled to undergo general anesthesia requiring tracheal intubation for elective surgery Exclusion criteria included a gross anatomical abnormality before surgery of the head neck and cervical spine previously difficult tracheal intubation loose teeth or those requiring a rapid sequence or awake intubation moderate or severe obstructiverestrictive pulmonary disease accompanied by pulmonary function tests Anesthesia was induced with remifentanyl 3ngkg propopol 1-2 mgkg or TIVA 2 fresopol 4ugdL remifentanyl 3ngdL and rocuronium 08 mgkg to facilitate tracheal intubation Laryngoscopy was performed after the loss of the fourth twitch in the train-of-four in response to ulnar nerve stimulation All laryngoscopies using a 4 Macintosh blade were performed with the patient placed in the sniffing position Tracheal intubation was performed without assistance ex External laryngeal manipulation Used stylet A single experienced anesthesiologist blinded to each group performed all of the direct laryngoscopies and classified the laryngoscopic view according to the modified Cormack and Lehane grade measured number of attempts intubation time and blood pressure and heart rate before after intubation
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