Ignite Creation Date:
2024-05-06 @ 8:27 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06383494
Status:
RECRUITING
Last Update Posted:
2024-05-29
First Post:
2024-04-22
Brief Title:
GMA-TulipTM i-gelTM and the LMA-SupremeTM LMA-S Devices in Airway Management
Sponsor:
Zhejiang Cancer Hospital
Organization:
Zhejiang Cancer Hospital
Study Overview
Official Title:
GMA-TulipTM i-gelTM and the LMA-SupremeTM LMA-S Devices in Airway Management Under General Anesthesia a Randomized Controlled Study
Status:
RECRUITING
Status Verified Date:
2024-05
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:
Patients were randomly assigned to three extraglottic airway EGA devices groups for airway management after anesthesia induced Fiberoptic bronchoscope FB guided glottic exposure grading was performed and other airway management quality was recorded
Detailed Description:
Mechanical ventilation was volume controlled and time cycled with tidal volumes 6-8 mlkg set to maintain peak inspiratory pressures of less than 20 cm H2O and ventilatory frequency adjusted to maintain end-tidal carbon dioxide PETCO2 at 35-45 mmHg Then a fiberoptic bronchoscope was passed through airway tube into the device to perform glottic exposure grading Peak airway pressure incidence of pharyngalgia bleeding hoarseness and dysphagia were recorded
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