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NCT03089359 Clinical Trial

Prehospital Recognition and Identification of Unspecific Symptoms

Morality Clinical Trial

— PRIUS  

Official title:
Prehospital Recognition and Identification of Unspecific Symptoms

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03089359
Other study ID # PRIUS
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 4, 2015
Est. completion date March 23, 2021

Study information
Verified date March 2021
Source Karolinska Institutet
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluates the predictive value of soluvent urokinase plasminogen activator receptor (suPAR) and lactate with respect to serious conditions among patients presenting to the EMS with unspecific symptoms.

Recruitment information / eligibility
Status Completed
Enrollment 414
Est. completion date March 23, 2021
Est. primary completion date March 23, 2021
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Unspecific symptoms (not feeling well, decreased general health condition, unable to cope with usual daily activities, feeling weak) - Normal vital signs - Transported to ED - Able to give informed consent/ Next of kin gives informed consent Exclusion Criteria: - Specific symptoms - under 18 years of age - Stays home / other caregiver than ED - Referral from caregiver - No personal numer (social security number)

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Finland Helsinki University Helsinki
Sweden Karolinska Institute Stockholm

Sponsors (1)
Lead Sponsor Collaborator
Karolinska Institutet

Countries where clinical trial is conducted

Finland,  Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Serious condition Predefined serious condition During medical care event
Secondary Mortality 24h and 30 day mortality 24hours and 30 days
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