Establishment and validation of risk prediction model for hypoxemia in patients undergoing painless gastroscopy

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2400090759

Enrollment

Unknown

Registered

2024-10-12

Start date

2023-09-01

Completion date

Unknown

Last updated

2024-10-15

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

Conditions

patients undergoing painless gastroscopy

Interventions

Cipofol sedates:None

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients scheduled for painless gastroscopy examination; (2) Aged 18 years or above; (3) ASA classification: I-III; (4) Anesthesia with ciprofol.

Exclusion criteria

Exclusion criteria: (1) Individuals with severe organ dysfunction; (2) Individuals with coagulation disorders; (3) Individuals with hypoxemia prior to the examination (SpO2 < 90%); (4) Pregnant or lactating women; (5) Individuals who are allergic to the examination drugs; (6) Individuals who are allergic to soy;

Design outcomes

Primary

Measure	Time frame
hypoxemia;	—

Countries

China

Contacts

Public ContactXuetingting

Huaian First Hospital Affiliated to Nanjing Medical University

fay86051724@163.com+86 152 4025 9957

Outcome results

None listed

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