Anesthesia Crisis Resource Management in Standardized Training for Resident Physicians and Perioperative Anesthesia Safety

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2500104711

Enrollment

Unknown

Registered

2025-06-22

Start date

2025-06-30

Completion date

Unknown

Last updated

2025-06-30

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

Conditions

Perioperative anesthesia-related adverse events

Interventions

Case Group:None

Control Group:None

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing surgery under general anesthesia or regional anesthesia at the Xiehe Hospital affiliated to Fujian Medical University 2. Those who have signed the informed consent form and voluntarily participate in this study

Exclusion criteria

Exclusion criteria: 1. Patients who refused to participate in this trial 2. Allergic reactions occurred 3. Severe bleeding during surgery 4. Equipment-related issues

Design outcomes

Primary

Measure	Time frame
Anesthesia-related adverse events;	—

Secondary

Measure	Time frame
Common categories of anesthesia-related adverse events;	—

Countries

China

Contacts

Public ContactChen Shizhe

Fujian Medical University Union Hospital

695230021@qq.com+86 187 5912 3186

Outcome results

None listed

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