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Emergency Room Analgesia and Sedation Survey-2

Emergency Room Analgesia and Sedation Survey-2

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07152457
Acronym
EASY-2
Enrollment
13000
Registered
2025-09-03
Start date
2025-09-01
Completion date
2026-06-30
Last updated
2025-09-03

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

Conditions

Current Status of Analgesia and Sedation Cognition and Implementation

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.

Interventions

OTHERNo intervention

None intervention

Sponsors

Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 120 Years

Inclusion criteria

1. : 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. 2. 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.

Exclusion criteria

1. Pregnant women 2. patients undergoing end-of-life care 3. individuals incapable of providing informed consent 4. patients who decline participation.

Design outcomes

Primary

MeasureTime frameDescription
Cognitive scoreAt the time of inclusion in the studyThe cognitive scores obtained through questionnaire surveys

Contacts

Primary ContactZhongjun Zheng
drzheng@zju.edu.cn+8615869119921

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026