Ignite Creation Date:
2025-12-24 @ 9:23 PM
Ignite Modification Date:
2025-12-25 @ 7:09 PM
Study NCT ID:
NCT03542032
Status:
COMPLETED
Last Update Posted:
2019-07-05
First Post:
2018-05-18
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Comparison of I-Gel Laryngeal Mask Airway Placement Methods in Elective Surgery
Sponsor:
Ankara Diskapi Training and Research Hospital
Organization:
Study Overview
Official Title:
Comparison of I -Gel Mask Airway Placement Methods in Elective Surgery: Jaw Thrust Maneuver vs Conventional Technique
Status:
COMPLETED
Status Verified Date:
2018-05
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:
To compare the jaw thrust maneuver with the conventional technical methods to place the I-Gel laryngeal mask
Detailed Description:
Patients who underwent elective surgery under general anesthesia and who were between the ages of 18 and 75 and who had ASA score I-II-III would be included in the study. Patients' mallampati scores, thyromental distances, mouth openings will be recorded.
Patients will be divided into two groups according to supraglottic airway insertion method.
Both groups will record the insertion time of i-gel, number of trials, operative time, placement complications.
Recorded complications (blood, laryngospasm, etc.) during insertion and removal of supraglottic airway devices will be assessed.
Patients' postoperative sore throat will be questioned and recorded.
Patients will be divided into two groups according to supraglottic airway insertion method.
Both groups will record the insertion time of i-gel, number of trials, operative time, placement complications.
Recorded complications (blood, laryngospasm, etc.) during insertion and removal of supraglottic airway devices will be assessed.
Patients' postoperative sore throat will be questioned and recorded.
Study Oversight
Has Oversight DMC:
False
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?: