ClinicalTrials.Veeva

Menu

Prognostic Value of Lactates in ICU

M

Mongi Slim Hospital

Status

Completed

Conditions

Mortality

Treatments

Diagnostic Test: Blood lactate level

Study type

Observational

Funder types

Other

Identifiers

NCT04792736
Lactates ICU

Details and patient eligibility

About

he aim of this prospective, analytic trial was to evaluate the accuracy of blood lactates levels in predicting mortality in ICU patients.

Full description

In this study, conducted over o 12 months period, arterial blood lactates levels were measured in ICU patients at admission (H0), every 6 hours during the first day and and H48.

This trial included traumatic, medical and surgical patients requiring ICU stay for a predictive period > to 24 hours.

Blood lactates were evaluated as a prognostic parameter in predicting ICU mortality and compared to classic prognostic scores such as: SOFA score, IGS II and APACHE II.

The primary end point was ICU mortality.

Enrollment

135 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adults admissions in ICU with a predicted length of stay > 24 hours

Exclusion criteria

  • Patients who died during the first 24 hours after ICU admission

Trial design

135 participants in 2 patient groups

Survivors
Description:
Patients discharged alive from intensive care unit
Treatment:
Diagnostic Test: Blood lactate level
non survivors
Description:
Patients who succumbed during their ICU stay
Treatment:
Diagnostic Test: Blood lactate level

Trial contacts and locations

2

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems