ClinicalTrials.Veeva

Menu

Lactate Clearance According to the Presence of Hepatic Dysfunction

Samsung Medical Center logo

Samsung Medical Center

Status

Unknown

Conditions

Liver Failure
Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT01709565
SamsungMC

Details and patient eligibility

About

The purpose of this study is to compare lactate clearance in patients with severe sepsis and septic shock according to the presence of hepatic dysfunction.

Full description

Lactate clearance is well known to be associated with mortality in patients with severe sepsis and septic shock. To normalize lactate levels is one of important goals of early resuscitation of sepsis patients.

Lactate clearance can be changed by various factors including patient characteristics, severity of shock, and treatment. In particular, hepatic dysfunction might impair the clearance of lactate because liver is a principal organ for lactate metabolism. However, an association between lactate clearance and hepatic failure has not been evaluated during initial resuscitation of patients with severe sepsis and septic shock. The primary goal of this study is to compare lactate clearance in patients with severe sepsis and septic shock according to the presence of hepatic dysfunction. The secondary goal is to evaluate if lactate clearance is associated with mortality even in patients with hepatic dysfunction.

Enrollment

245 estimated patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients who presented with septic shock or severe sepsis within 6 hours after emergency department arrival

Exclusion criteria

  • Terminal malignancy or illness with a expected survival < 4 months
  • Patients who previously signed "Do Not Resuscitate" or "Do Not Intubate" orders
  • Patients who do not undergo the early goal-directed therapy

Trial design

245 participants in 2 patient groups

No hepatic dysfunction
Description:
No hepatic dysfunction, total plasma bilirubin ≤ 2.0 mg/dl
Hepatic dysfunction
Description:
Hepatic dysfunction, total plasma bilirubin \> 2.0 mg/dl

Trial contacts and locations

1

Loading...

Central trial contact

Ik Joon Jo, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems