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Status unknownNCT03217981HUVRUpdated Aug 4, 2017

Sepse: Critical Analysis of New Sepse Definitions and Retrospective Evaluation of Sepse Protocol at a Tertiary Hospital in Brazil

An observational study in Sepsis, sponsored by Unimed Volta Redonda. Status unknown at 1 site in Brazil. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-08-04.

Sponsored by Unimed Volta Redonda · Observational

The sponsor has not verified this record recently (last verified Aug 2017), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
506
Ages
18 Years and older
Sex
All
01

Study summary

Research in the databases Lilacs, BIREME, SciELO by the terms: systemic inflammatory response syndrome (SIRS), sepsis, severe sepsis and septic shock and their equivalents in the English language. Selection of the main articles of the last five years to study and contextualize the reality presented since the implantation of the HUVR sepsis protocol. Statistical analysis of data since the implementation of the sepsis protocol in the HUVR, in July 2014 until June 2016.

02

Conditions studied

  • Sepsis
03

In context

Lead sponsor

This is the only study on the registry with Unimed Volta Redonda as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients over 18 years of age hospitalized with suspected or confirmed diagnosis of sepsis at HUVR.

Inclusion criteria

All individuals who had a confirmed or suspected sepsis diagnosis and had a sepsis protocol completed during the study period.

Exclusion criteria

-

Exclusion Criteria:

Individuals with confirmed or suspected sepsis in the study period who did not complete the protocol.

Individuals under the age of 18

-

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
506 participants (estimated)
Patient registry
No

Groups and cohorts

  • 2015

    2015 - Individuals with a diagnosis of sepsis from June 2014 to May 2015

    Other: Sepsis protocol

  • 2016

    2016 -Individuals with a diagnosis of sepsis from June 2015 to May 2016

    Other: Sepsis protocol

Interventions

  • OtherSepsis protocol

    Adherence to the sepsis protocol

06

What researchers measure

Primary outcomes

  1. Adherence to the sepsis protocol

    Implementation of the measures recommended in the sepsis protocol

    Time frame: From 2014 to 2016

Secondary outcomes

  1. Sepsis mortality rate

    Assessment of the evolution of the sepsis mortality rate

    Time frame: From 2014 to 2016

07

Study locations

1 of 1 sites recruiting
  • Vicente Lopes
    Volta Redonda, Rio de Janeiro 27258-000, Brazil
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 4, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03217981
Lead sponsor
Unimed Volta Redonda
Responsible party
Vicente Lopes da Silva Junior (Principal Investigator, Unimed Volta Redonda) — Principal investigator
First posted
Jul 14, 2017
Start date
Aug 2, 2017
Primary completion
Aug 5, 2017 (estimated)
Completion
Aug 8, 2017 (estimated)
Last update
Aug 4, 2017

Study contacts

Vicente L da Silva Jr
Contact
vicente.junior@unimedvr.com.br
+5521981227376
Leila Auler
study director · Director

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

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