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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03601767
Other study ID # 38788/2017
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 20, 2017
Est. completion date August 1, 2019

Study information

Verified date July 2018
Source Azienda Ospedaliera San Paolo
Contact Livio Colombo, MD
Phone +390281844250
Email livio.colombo@asst-santipaolocarlo.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of the present study is to develop a prognostic tool to assess the risk of dead and major complications in patient admitted to hospital for infection. A detailed database of clinical, biochemical and microbiological data is recorded and each item is analyzed and compared with clinical outcomes to develop a prognostic score.


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date August 1, 2019
Est. primary completion date January 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- al least 18 years old

- admission to hospital for any infection for more than 72 hours

Exclusion Criteria:

- pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Ospedale San Paolo Polo Univesitario - ASST Santi Paolo e Carlo Milan

Sponsors (1)

Lead Sponsor Collaborator
Azienda Ospedaliera San Paolo

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality at 28 days
Secondary major complications at 28 days
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