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Investigation and Research on the Cognition and Implementation Status of Analgesia and Sedation in Emergency Resuscitation Rooms in China

Investigation and Research on the Cognition and Implementation Status of Analgesia and Sedation in Emergency Resuscitation Rooms in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500111851
Enrollment
Unknown
Registered
2025-11-06
Start date
2025-11-15
Completion date
Unknown
Last updated
2025-11-11

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

Conditions

Sedation

Interventions

Investigation and Research on the Cognitive Status of Analgesia and Sedation among Medical Staff in Emergency Resuscitation Rooms in China - A Cross-sectional Study (Part One:None
The Implementation status of Analgesia and Sedation in Emergency Resuscitation rooms in China - Cohort Study (Part Two):None

Sponsors

The Second Affiliated Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Part 1 Inclusion Criteria: (1) Medical staff on the payroll of the emergency department who are actually working in the emergency rescue room; (2) Have been engaged in emergency work for at least 1 year; (3) Voluntarily participate in investigation and research. Each unit should include at least 12 medical staff members (6 doctors and 6 nurses), among whom 3 should have junior professional titles and 3 should have intermediate or higher professional titles respectively. Part 2 Inclusion Criteria: All adult patients (aged 18 years or older) admitted to the emergency resuscitation room from November 15, 2025 to June 30, 2026.

Exclusion criteria

Exclusion criteria: Part One Exclusion Criteria: 1. Those who are unable to sign informed consent; 2. Reject participants. Part Two Exclusion Criteria 1. Pregnant women; 2. Hospice care patients; 3. Those who are unable to sign informed consent; 4. Patients who refuse to participate.

Design outcomes

Primary

MeasureTime frame
Cognitive score;Current implementation status;

Countries

China

Contacts

Public ContactZheng Zhongjun

The Second Affiliated Hospital of Zhejiang University School of Medicine

drzheng@zju.edu.cn+86 571 8778 3921

Outcome results

None listed

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