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NCT03217981: HUVR

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

Status unknown Last updated 4 August 2017
What this trial tests

trial testing Sepsis protocol in Sepsis in 506 participants. Status unknown.

Timeline
2 August 2017
Primary endpoint
5 August 2017
8 August 2017

Quick facts

Lead sponsorUnimed Volta Redonda
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment506
Start date2 August 2017
Primary completion5 August 2017
Estimated completion8 August 2017
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Unimed Volta Redonda

Who can join

18 and older, any sex, with Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sepsis

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03217981.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing