Actively Recruiting
Rapid Response Teams - How and Who?
Led by Nordsjaellands Hospital · Updated on 2025-09-17
1500
Participants Needed
1
Research Sites
230 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This will be an investigator initiated One-sided blinded Randomized Clinical Trial. The study will examine the composition of the Rapid Response Team (RRT). the investigators will examine to see if a Critical Care Outreach Team (CCOT) consisting of an ICU-Nurse and a general ward physician and nurse are non-inferior to a Medical Emergency Team (MET) consisting of an ICU-Doctor and ICU Nurse as well as a general ward physician and nurse. The randomization will be done using an Analogue randomization sequence using sealed opaque envelopes with central randomization.The experimental intervention will be the CCOT. The statistical analyses will be done on the primary outcomes in the intention to treat population and on the secondary outcomes on an per-protocol basis exempting those with protocol violations.
CONDITIONS
Official Title
Rapid Response Teams - How and Who?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Admitted to any general ward of the hospital
- Aged 18 years or older
- In need of Rapid Response Team attention
You will not qualify if you...
- Younger than 18 years old
- Admitted to the delivery ward
- Admitted to any ward in the anesthetic department, including ICU, High Dependency Unit, Post Operation Department, Operating Theatre, or Same Day Surgery Admissions
- Not admitted at the time of Rapid Response Team call, such as evaluation track in Emergency department, Out-Patient departments, or X-ray department
- Any patient who cannot be randomized at the time of call
AI-Screening
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Trial Site Locations
Total: 1 location
1
Nordsjællands Hospital
Hillerød, Danmark, Denmark, 3400
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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