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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03740802
Other study ID # PORPOISE2-REA (29BRC18.0022)
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 26, 2018
Est. completion date April 9, 2018

Study information

Verified date January 2018
Source University Hospital, Brest
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective study in the surgical intensive care unit of the Brest Teaching Hospital (France) during a 6-months period (January 2015 -May 2015) to study the independent association between hypophosphatemia and 28-day infection.


Recruitment information / eligibility

Status Completed
Enrollment 264
Est. completion date April 9, 2018
Est. primary completion date April 9, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adults

Exclusion Criteria:

- Less than 18 years old

- Infected at admission

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 Number of patients with sepsis within 28 days after ICU admission Sepsis was defined according to the criteria of the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3). 28 days since the ICU admission
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