Emergency Room Analgesia and Sedation Survey-2

NCT07152457 | Not Yet Recruiting

• 2 other identifiers: 2025-0530No funding is currently availa
• Study Type: observational
• Target: 13,000
• Locations: 0 countries
• Sites: N/A

Brief Summary

Part 1: Assessment of Healthcare Providers' Knowledge on Analgesia and Sedation in Emergency Resuscitation Rooms Across China This study aims to evaluate the understanding of healthcare providers in emergency resuscitation rooms regarding the principles of analgesia and sedation, commonly used assessment tools, and delirium management, and to identify key factors that may influence their level of knowledge. Part 2: Implementation Practices of Analgesia and Sedation in Emergency Resuscitation Rooms Across China: A Multicenter Prospective Cohort Study Primary Objective: To assess the extent of adherence to standardized protocols for analgesia and sedation in emergency resuscitation rooms of general hospitals in China. Secondary Objectives: (1) To identify key factors affecting compliance with standardized analgesia and sedation practices in emergency resuscitation settings, thereby providing evidence for targeted interventions; (2) To examine the impact of analgesia and sedation implementation on clinical outcomes and prognosis of patients in emergency resuscitation rooms.

Conditions

Current Status of Analgesia and Sedation Cognition and Implementation

Outcome Measures

Primary Outcomes (1)

• Cognitive score

  The cognitive scores obtained through questionnaire surveys

  At the time of inclusion in the study

Interventions

No intervention OTHER

None intervention

Eligibility Criteria

• Age: 18 Years - 120 Years
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Patients over the age of 18 who were treated in the emergency rescue room

You may qualify if:

• ： Part 1: (1) Healthcare professionals currently assigned to the emergency department and actively working in the emergency resuscitation room; (2) With at least one year of clinical experience in emergency medicine; (3) Willing to voluntarily participate in the investigation. Each participating institution is required to enroll a minimum of 12 healthcare providers, including at least 6 physicians and 6 nurses. Within each group (physicians and nurses), at least 3 participants must hold junior professional titles and at least 3 must hold intermediate or senior-level professional titles.
• Part 2: All adult patients (≥18 years of age) admitted to the emergency resuscitation room during the period from July 15, 2025 to July 30, 2025.

You may not qualify if:

• Pregnant women
• patients undergoing end-of-life care
• individuals incapable of providing informed consent
• patients who decline participation.

Sponsors & Collaborators

• Second Affiliated Hospital, School of Medicine, Zhejiang University: lead

Central Study Contacts

Zhongjun Zheng

CONTACT

+8615869119921; drzheng@zju.edu.cn

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: CROSS SECTIONAL
• Target Duration: 1 Day
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 26, 2025
• First Posted: September 3, 2025
• Study Start: September 1, 2025
• Primary Completion (Estimated): June 30, 2026
• Study Completion (Estimated): June 30, 2026
• Last Updated: September 3, 2025

Record last verified: 2025-08