Current Status of Analgesia and Sedation Cognition and ImplementationEASY-2NCT07152457
Emergency Room Analgesia and Sedation Survey-2
An observational study of Current Status of Analgesia and Sedation Cognition and Implementation, run by Second Affiliated Hospital, Zhejiang University, School of Medicine.
Trial 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… Read more about this study
- Who is it for?
- Ages 18 to 120 years
- Conditions the study is for
- Current Status of Analgesia and Sedation Cognition and Implementation
- How many people
- 13,000 participants
- Where
- No sites listed yet
- Study dates
- 1 Sep 2025to 30 Jun 2026
- How long will I take part?
- 1 Day
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 120 years
- All sexes
- Adult, Older adult
Study population: Patients over the age of 18 who were treated in the emergency rescue room
Who may be able to join
- ： 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.
Who cannot join
- Pregnant women
- patients undergoing end-of-life care
- individuals incapable of providing informed consent
- patients who decline participation.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
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.
- Being tested
- No intervention
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
No interventionOther
None intervention
What is being measured
The primary outcome is the main question the study is designed to answer.
Cognitive score
The cognitive scores obtained through questionnaire surveys
Measured: At the time of inclusion in the study
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Sep 2025
- Study start1 Sep 2025 (estimated)
- Primary completion30 Jun 2026 (estimated)
- Study completion30 Jun 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Current Status of Analgesia and Sedation Cognition and ImplementationStudies of the same condition, open and under way.
- More trials run by Second Affiliated Hospital, Zhejiang University, School of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 13,000 participants (estimated)
- Target duration
- 1 Day
Sponsor and investigators
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07152457
- Sponsor's protocol ID
- 2025-0530
- Other IDs
- No funding is currently availa
- Acronym
- EASY-2
- Status last verified
- Aug 2025
- First submitted
- 26 Aug 2025
- Last updated
- 3 Sep 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 3 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Emergency Room Analgesia and Sedation Survey-2
- ClinicalTrials.gov ID
- NCT07152457
- Acronym / sponsor ID
- EASY-2 / 2025-0530
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 13,000 participants (estimated)
- Lead sponsor
- Second Affiliated Hospital, Zhejiang University, School of MedicineUniversity, hospital or other
- Study start
- 1 Sep 2025 (estimated)
- Primary completion
- 30 Jun 2026 (estimated)
- Study completion
- 30 Jun 2026 (estimated)
- First posted
- 3 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Target follow-up
- 1 Day
Who may qualify
- Ages
- 18 to 120 years
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Patients over the age of 18 who were treated in the emergency rescue room
Key inclusion criteria (2 listed)
- ： 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.
Key exclusion criteria (4 listed)
- Pregnant women
- patients undergoing end-of-life care
- individuals incapable of providing informed consent
- patients who decline participation.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| No interventionNone intervention | Other | – |
Primary outcome
Cognitive score
Time frame: At the time of inclusion in the study
The cognitive scores obtained through questionnaire surveys
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Sep 2025.
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Questions about this trial
What is this clinical trial studying?
An observational study of Current Status of Analgesia and Sedation Cognition and Implementation, run by Second Affiliated Hospital, Zhejiang University, School of Medicine.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 3 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Zhongjun Zheng (+8615869119921, drzheng@zju.edu.cn), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Cognitive score (time frame: At the time of inclusion in the study). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Sep 2025.