Effect of Sepsis Response Team in the Emergency Department
Prospective Cohort Study Examining the Effect of a Sepsis Rapid Response Team in the Emergency Department
1 other identifier
observational
245
1 country
1
Brief Summary
Does sepsis response team in the emergency department increase the portion of sepsis patient who receive adequate treatment within one hour?
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started May 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 15, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 15, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2018
CompletedFirst Submitted
Initial submission to the registry
December 27, 2018
CompletedFirst Posted
Study publicly available on registry
December 31, 2018
CompletedMay 3, 2022
April 1, 2022
1 year
December 27, 2018
April 27, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
Time from arrival the emergency department to antibiotic is given.
Time from arrival the emergency department to antibiotic is given.
6 months
Study Arms (2)
Before of sepsis rapid response team
Time from arrival at the Emergency Department to antibiotic is administered, before introduction of sepsis response team in the Emergency Department.
Sepsis rapid response team
Time from arrival at the Emergency Department to antibiotic is administered, with sepsis response team in the Emergency Department.
Interventions
Patients with suspected sepsis is managed by a sepsis rapid response team in a structured manner.
Eligibility Criteria
Adult patients with suspected sepsis in emergency department
You may qualify if:
- Patients with suspected sepsis
You may not qualify if:
- Patients who was consider not to need antibiotics
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Oslo University Hospital
Oslo, 0424, Norway
Related Publications (1)
Trydal E, Martinsen AB, Beisland F, Jacobsen D, Holten AR. [Structured evaluation on arrival of patients with sepsis and initiation of antibiotics]. Tidsskr Nor Laegeforen. 2019 May 27;139(9). doi: 10.4045/tidsskr.18.0216. Print 2019 May 28. Norwegian.
PMID: 31140244RESULT
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Aleksander Holten, Phd, MD
Oslo University Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Consultant Physician
Study Record Dates
First Submitted
December 27, 2018
First Posted
December 31, 2018
Study Start
May 15, 2017
Primary Completion
May 15, 2018
Study Completion
May 15, 2018
Last Updated
May 3, 2022
Record last verified: 2022-04
Data Sharing
- IPD Sharing
- Will not share