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Clinical Trial 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


Clinical Trial 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 Design


Related Conditions & MeSH terms

  • Perioperative Respiratory Adverse Events

NCT number NCT06354569
Study type Observational
Source Sichuan Provincial People's Hospital
Contact Yanyu Liu
Phone +8613438348895
Email 43197113@qq.com
Status Recruiting
Phase
Start date December 31, 2024
Completion date December 31, 2024

See also
  Status Clinical Trial Phase
Withdrawn NCT03996343 - Airway Management and Weight in Children N/A