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Outcome Predictors in Patients With Severe Sepsis and Optimized Central Venous Oxygen Saturation

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National Taiwan University

Status

Completed

Conditions

Sepsis

Treatments

Other: Determined by intended physician

Study type

Observational

Funder types

Other

Identifiers

NCT01362829
200907064R
098014-3 (Other Identifier)

Details and patient eligibility

About

The investigators perform a prospective observation study to search for the outcome predictors (ScvO2 and lactate) in patients with severe sepsis after admission to ICU.

Full description

Early goal-directed therapy in patients with severe sepsis or septic shock was found to provide survival benefit.It was thought that early optimization of ScvO2 within 6 hours in emergency department brought survival benefit to patients of septic shock or severe sepsis.On the other hand, early lactate clearance is associated with improved outcome in patients with severe sepsis or septic shock. In patients with severe sepsis and septic shock, those with low lactate clearance had poor prognosis, despite optimization of ScvO2. It is unknown if ScvO2 could still guide hemodynamic resuscitation after admission into ICU. The investigators perform a prospective observation study to see the correlation between ScvO2 and clinical outcome (including organ failure, disease severity, and survival) and the correlation between lactate and clinical outcome. Furthermore, if ScvO2 >= 70% is still of prognostic significance in ICU, we will investigate the outcome in patients with high ScvO2 and high serum lactate levels, and to evaluate the clinical features of this patient population.

Enrollment

90 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult patients who are admitted to medical intensive care units with severe sepsis or septic shock

Exclusion criteria

  • Patients would be excluded if they have any one of the exclusion criteria, *including pregnancy

    • presence of acute cerebral vascular attack
    • acute cardiogenic lung edema
    • status asthmatics
    • cardiac dysrhythmia as the primary diagnosis
    • massive gastrointestinal bleeding
    • epileptics
    • drug overdose
    • requirement of immediate surgery
    • hematologic malignancies
    • febrile neutropenia
    • treatment with immunosuppressive agents before admission
    • advanced malignancy and poor pre-admission performance status
    • with inevitable short-term mortality or morbidity
    • HIV infection
    • refusal of consent

Trial design

90 participants in 1 patient group

Patients with severe sepsis
Description:
Patients who are admitted to medical ICU with severe sepsis
Treatment:
Other: Determined by intended physician

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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