Triage of Abdominal Pain in the Emergency Department
Evaluation of Triage Criteria for Abdominal Pain in the Emergency Department
1 other identifier
observational
4,000
1 country
1
Brief Summary
The investigators aim to evaluate in a retrospective study the performance of the Swiss Emergency Triage Scale to identify at the door of the Emergency Department patients requiring emergent intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2014
Typical duration 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
First Submitted
Initial submission to the registry
December 12, 2013
CompletedFirst Posted
Study publicly available on registry
February 17, 2014
CompletedStudy Start
First participant enrolled
March 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2017
CompletedJuly 27, 2017
July 1, 2017
3.8 years
December 12, 2013
July 26, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Emergency intervention
Emergency intervention is a composite outcome of: emergency surgical intervention or radiological intervention or emergent endoscopy
participants will be followed for the duration of hospital stay, an expected average of 2 weeks
Secondary Outcomes (1)
Time to medical evaluation
participants will be followed for the duration of emergency department stay, an expected average of 5 hours
Study Arms (1)
Patients with abdominal pain
Adult patients admitted to the Emergency Department with a main complaint of abdominal pain
Eligibility Criteria
Adults (\> 16 y) admitted with abdominal pain in the Emergency Departement of a primary and tertiary teaching urban hospital.
You may qualify if:
- \>= 16 y
- abdominal pain as the main complaint
You may not qualify if:
- none
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Geneva University Hospitals
Geneva, 1211, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Olivier T Rutschmann, MD, MPH
University Hospital, Geneva
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MD, MPH
Study Record Dates
First Submitted
December 12, 2013
First Posted
February 17, 2014
Study Start
March 1, 2014
Primary Completion
December 1, 2017
Study Completion
December 1, 2017
Last Updated
July 27, 2017
Record last verified: 2017-07