Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06943885

Comparison of 5G-Mobile Stroke Unit With Standard EMS for Acute Ischemic Stroke

Led by Beijing Emergency Medical Center · Updated on 2025-05-14

952

Participants Needed

1

Research Sites

218 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

While Mobile Stroke Units (MSUs) are considered as a relatively new model for acute stroke treatment, 5G Mobile Stroke Units (5G MSUs) have already come into service for stroke treatment in some parts of China. Since limited evidence has been found to suggest their advantages over conventional Emergency Medical Services (EMS), well-conducted clinical studies are required to further assess their effectiveness and safety. This study aims to evaluate whether 5G MSUs outperform standard management (SM) by EMS in terms of functional outcomes of acute ischemic stroke (AIS) patients within 4.5 hours after symptom onset in urban and rural areas of China.

CONDITIONS

Official Title

Comparison of 5G-Mobile Stroke Unit With Standard EMS for Acute Ischemic Stroke

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  1. History and physical/neurological examination consistent with acute stroke.
  2. Age≥18.
  3. Last seen normal within 4hr 30 min of symptom onset.
  4. Pre-stroke modified Rankin scale ≤3（Being able to ambulate）.
  5. No rt-PA/TNK exclusions per guidelines, prior to CT scan or baseline labs.
  6. Informed consent obtained from patient (if competent) or legal representative.
Not Eligible

You will not qualify if you...

  1. Malignant or other severe primary disease with life expectancy <1 year.
  2. Participation in other interventional randomized clinical trials within 3 months before enrollment.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Beijing Emergency Medical Center

Beijing, Beijing Municipality, China, 100031

Actively Recruiting

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Research Team

J

Jie Zhou, MD

CONTACT

D

Dou Li, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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