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NCT03529058 Clinical Trial

Hypophosphatemia as a Predictive Marker of Mortality During Sepsis in ICU

Infection Clinical Trial

— PORPOISE-REA  

Official title:
Evaluation of Hypophosphatemia as a Predictive Marker of Mortality During Sepsis in ICU

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03529058
Other study ID # PORPOISE-REA ( 29BRC17.0180)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 26, 2017
Est. completion date March 31, 2018

Study information
Verified date November 2017
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective study in the 3 intensive care units of the Brest Teaching Hospital (France) during a 18-months period (June 2014 -December 2015) to study the independent association between hypophosphatemia and 90-day mortality.

Recruitment information / eligibility
Status Completed
Enrollment 193
Est. completion date March 31, 2018
Est. primary completion date March 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Blood stream infection

Exclusion Criteria:

- Less than 18 years old

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France CHRU de Brest Brest

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Brest

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary 90-day mortality 90 days since the first blood stream infection in ICU
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