Predicting Sedation-Related Adverse Events in Patients Undergoing Painless Gastroscopy Based on Explainable Machine Learning Algorithms

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300079175

Enrollment

Unknown

Registered

2023-12-26

Start date

2024-01-15

Completion date

Unknown

Last updated

2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sedation-Related Adverse Events in Patients Undergoing Painless Gastroscopy

Interventions

Sedation-Related Adverse Events in Patients Undergoing Painless Gastroscopy:None

Eligibility

Sex/Gender

All

Age

18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1) Aged 18 years or above; 2) ASA (American Society of Anesthesiologists) anesthesia risk levels I to II; 3) Patients scheduled for elective gastroscopy; 4) Patients able to undergo sedation with propofol.

Exclusion criteria

Exclusion criteria: 1) Patients with sleep apnea syndrome; 2) Patients with difficult airway management; 3) Patients with significant gastric emptying dysfunction; 4) Patients with acute gastrointestinal bleeding; 5) Patients with neuropsychiatric disorders; 6) Pregnant women; 7) Patients allergic to egg yolk or soybean oil (may be allergic to propofol); 8) Patients who do not agree to sign the informed consent form.

Design outcomes

Primary

Measure	Time frame
Sedation-Related Adverse Events in Patients Undergoing Painless Gastroscopy;	—

Countries

China

Contacts

Public ContactXiaowei Jin

Wenzhou Integrated Traditional Chinese and Western Medicine Hospital

xiaoweijinwz@163.com+86 139 5871 8529

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026