Tokyo, June 17 -- UMIN Clinical Trials Registry (UMIN-CTR) received information related to the study (UMIN000061937) titled 'Comparison of the effect of the use of the i-gel, a supraglottic device, on airway clearance and effectiveness in patients in the lateral position' on June 17.
Study Type:
Observational
Primary Sponsor:
Institute - Seirei Kikataghara General Hospital
Condition:
Condition - Surgical patients
Classification by malignancy - Others
Genomic information - NO
Objective:
Narrative objectives1 - The current study aims to investigate the utility of a new i-gel by comparing it with the classic i-gel during mechanical ventilation in the lateral decubitus position.
Basic objectives2 - Safety
Eligibility:
Age-lower limit - 20
years-old
<=
Age-upper limit - Not applicable
Gender - Male and Female
Key inclusion criteria - Patients undergoing a scheduled surgery under general anesthesia
Key exclusion criteria - Patients who preferred tracheal intubation.
Patient without the use of neuromuscular blocking agents.
Patients for whom intravenous anesthetic induction was contraindicated.
Target Size - 100
Recruitment Status:
Recruitment status - No longer recruiting
Date of protocol fixation - 2024 Year 12 Month 16 Day
Date of IRB - 2024 Year 12 Month 16 Day
Anticipated trial start date - 2025 Year 08 Month 01 Day
Last follow-up date - 2026 Year 12 Month 31 Day
To know more, visit https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000070864
Disclaimer: Curated by HT Syndication.
