New 3-Minute nursing assessment could speed up emergency care for critically ill patients

NCT ID NCT07249151

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a new 3-minute nursing assessment for emergency patients. Nurses checked vital signs and consciousness, then calculated a risk score to guide care. The goal was to see if this helps doctors start treatment faster for high-risk patients. The study involved 200-300 adults with acute illnesses like severe infection or heart failure.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could lead to faster, more accurate emergency care for critically ill patients, potentially reducing deaths and hospital stays.
What could go wrong
This is an observational study, not a treatment trial. It only tests a new assessment method, so it cannot directly improve outcomes. Results may not apply to all hospitals.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

1,000 people

The number who actually took part.

Started

May 2024

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 80 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Patients will be eligible for enrollment if they meet all of the following conditions: 1. Age between 18 and 80 years at the time of presentation. 2. Presentation to the emergency department (ED) for acute medical evaluation. 3. Completion of at least one documented Early Warning Score (EWS) assessment upon ED admission or during the ED stay. Exclusion Criteria: Patients will be excluded if they meet any of the following criteria: 1. Do-not-resuscitate (DNR) orders or enrollment in a palliative/comfort care pathway at the time of presentation. 2. Cardiac arrest upon arrival to the ED (unresponsive, pulseless, requiring resuscitation without return of spontaneous circulation). 3. Transfer out of the hospital (to another institution or to the operating room for immediate surgery) within 24 hours of ED admission. 4. History of major cardiac surgery (e.g., coronary artery bypass grafting, valve replacement) or heart transplantation, as these conditions may alter baseline hemodynamics and limit EWS applicability. 5. Severe chronic organ dysfunction, including: End-stage renal disease requiring maintenance dialysis; Severe hepatic insufficiency (Child-Pugh class C or equivalent); Advanced heart failure (New York Heart Association class IV). 6. Known allergy or contraindication to iodinated contrast media (if relevant laboratory or imaging assessments are required for outcome evaluation). 7. Pregnancy, due to altered physiological parameters and ethical considerations. 8. Incomplete or missing clinical records, preventing calculation of EWS or confirmation of study endpoints. 9. Duplicate enrollment due to repeated ED visits or readmissions during the study period (only the first eligible admission will be included).

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Acute critical illnesses in emergency settings are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Wuxi Taihu Hospital; Affiliated Hospital of Jiangnan University; Wuxi Binhu District Traditional Chinese Medicine Hospital; Wuxi Xinwu District Traditional Chinese Medicine Hospital

    Wuxi, Jiangsu, 214122, China