Suspended

PROGNOSTIC EVALUATION OF SEVERE SEPSIS AND SEPTIC SHOCK. PROCALCITONIN VERSUS DELTA SOFA

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What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Infections+5

+ Inflammation

+ Pathologic Processes

Over 18 Years
+4 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: May 2012
See protocol details

Summary

Principal SponsorHospital Sao Domingos
Study ContactJOSE R AZEVEDO, MDMore contacts
Last updated: April 26, 2013
Sourced from a government-validated database.Claim as a partner

Study start date: May 1, 2012

Actual date on which the first participant was enrolled.

This is a cohort prospective observational study that will include adult patients admitted to a multidisciplinary ICU of a tertiary hospital.

NCT01841190
Principal SponsorHospital Sao Domingos
Study ContactJOSE R AZEVEDO, MDMore contacts
Last updated: April 26, 2013
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

128 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

InfectionsInflammationPathologic ProcessesShockPathological Conditions, Signs and SymptomsSystemic Inflammatory Response SyndromeShock, SepticSepsis

Criteria

2 inclusion criteria required to participate
Adult patients admitted to the ICU
severe sepsis and septic shock
2 exclusion criteria prevent from participating
Children
Pregnant

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 2 locations

Recruiting

Hospital Sao Domingos

São Luís, BrazilOpen Hospital Sao Domingos in Google Maps
Recruiting

Hospital Sao Domingos

São Luís, Brazil
Suspended2 Study Centers