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Clinical Trials/NCT03217981
NCT03217981UnknownNot Applicable

Sepse: Critical Analysis of New Sepse Studies and Definitions and Retrospective Evaluation of Sepse Protocol Implementation at Hospital Unimed Volta Redonda

Unimed Volta Redonda1 site in 1 country506 target enrollmentStarted: August 2, 2017Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
506
Locations
1
Primary Endpoint
Adherence to the sepsis protocol

Study Overview

Brief 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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

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

Exclusion Criteria

  • •Individuals with confirmed or suspected sepsis in the study period who did not complete the protocol.
  • •Individuals under the age of 18

Outcomes

Primary Outcomes

Adherence to the sepsis protocol

Time Frame: From 2014 to 2016

Implementation of the measures recommended in the sepsis protocol

Secondary Outcomes

  • Sepsis mortality rate(From 2014 to 2016)

Investigators

Sponsor
Unimed Volta Redonda
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Vicente Lopes da Silva Junior

Principal Investigator

Unimed Volta Redonda

Study Sites (1)

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