Viewing Study NCT06354569



Ignite Creation Date: 2024-05-06 @ 8:22 PM
Last Modification Date: 2024-10-26 @ 3:26 PM
Study NCT ID: NCT06354569
Status: RECRUITING
Last Update Posted: 2024-04-09
First Post: 2024-04-03

Brief Title: Risk Factors and Risk Grading Prediction of Perioperative Respiratory Adverse Events in Children
Sponsor: Sichuan Provincial Peoples Hospital
Organization: Sichuan Provincial Peoples Hospital

Study Overview

Official Title: Risk Factors and Risk Grading Prediction of Perioperative Respiratory Adverse Events in Children
Status: RECRUITING
Status Verified Date: 2024-04
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 explore the risk factors of perioperative respiratory adverse events in children and to establish a risk prediction model of perioperative respiratory adverse events in children
Detailed Description: 600 children undergoing elective surgery under general anesthesia were selected Age sex weight height allergy history past history snoring passive smoking abnormal laboratory examination and chest X-ray before operation upper respiratory tract infection 14 days before operation Operation Site working years of anesthesiologist anesthesia method Operation Duration anesthesia duration perioperative vital signs and respiratory adverse events were collected The risk prediction model of perioperative respiratory adverse events in children was established by using LASSO least absolute shrinkage and selection operator algorithm and gradient boosting machine GBM algorithm to screen the relevant data collected during routine diagnosis and treatment such as demographic characteristics physical conditions airway sensitivity environmental sensitivity and anesthesia management

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