CClinicalTrials.gg
CompletedNCT06887439Updated Jan 21, 2026

Association of EASIX in Sepsis

An observational study in Sepsis, Septic Shock and Septic Syndrome, sponsored by Sisli Hamidiye Etfal Training and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-21.

Sponsored by Sisli Hamidiye Etfal Training and Research Hospital · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
150
Ages
18 Years and older
Sex
All
01

Study summary

This prospective study aims to determine the relationship between the EASIX score and mortality and prognosis in sepsis.

Read the detailed description

Sepsis is a life-threatening condition characterized by a dysregulated host response to infection, leading to organ dysfunction. Despite advancements in medicine, sepsis remains a significant cause of death worldwide. An international study showed that 48.9 million sepsis cases were diagnosed in 195 countries between 1990 and 2017, resulting in 11 million deaths. Recent studies have demonstrated that early diagnosis and treatment reduce sepsis mortality. Therefore, research has focused on identifying biomarkers that aid in early diagnosis and prognosis.

The Endothelial Activation and Stress Index (EASIX) was first defined by Luft et al. as a biomarker reflecting endothelial damage. Calculated using readily available laboratory parameters-serum lactate dehydrogenase (LDH) level (U/L) x creatinine level (mg/dL) / platelet count (10⁹/L)-it has been commonly used to predict mortality and prognosis in hematological malignancies. Recently, its application in predicting sepsis mortality and prognosis has gained attention, although only limited retrospective studies have been published.

02

Conditions studied

  • Sepsis
  • Septic Shock
  • Septic Syndrome

Keywords

  • sepsis
  • septic shock
  • endothelium
03

In context

Sepsis

1,899 studies on the registry are indexed under Sepsis; 462 are open to participants now.

This study's enrollment of 150 is close to the median of 160 across 931 observational studies indexed under Sepsis.

Browse Sepsis studies →

Lead sponsor

Sisli Hamidiye Etfal Training and Research Hospital is the lead sponsor of 110 studies on the registry; 14 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients (≥18 years old) diagnosed with sepsis were included.

Inclusion criteria

    • Patients diagnosed with sepsis during intensive care admission or admitted to intensive care with a diagnosis of sepsis

      • All patients over the age of 18

Exclusion criteria

Exclusion Criteria:

    • Patients under the age of 18

      • Patients with a history of multiple intensive care admissions
      • Patients who died within 24 hours of diagnosis
      • Patients diagnosed with CRF or currently treated for ARF
      • Patients with deficient serum creatinine, LDH and platelet values at the time of diagnosis Patients for whom consent could not be obtained from themselves or their relatives
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
150 participants (actual)
Target follow-up
18 Months
Patient registry
Yes

Groups and cohorts

  • sepsis group

    Adult patients (≥18 years old) diagnosed with sepsis

06

What researchers measure

Primary outcomes

  1. mortality

    The primary finding of the study was 28-day mortality after sepsis diagnosis

    Time frame: 28 days

Secondary outcomes

  1. Septic shock

    Septic shock was defined according to the SEPSIS-3 guidelines as the need for vasopressors or inotropes in patients diagnosed with sepsis.

    Time frame: 28 days

  2. Acute kidney injury

    Acute kidney injury was defined according to KDIGO guidelines as a ≥0.3 mg/dL increase in serum creatinine over 48 hours, a ≥1.5-fold increase in serum creatinine over 7 days, or urine output \<0.5 mL/kg/hour for 6 consecutive hours.

    Time frame: 28 days

07

Study locations

1 site
  • Sisli etfal research and training hospital
    Istanbul, 34371, Turkey (Türkiye)
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 21, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06887439
Lead sponsor
Sisli Hamidiye Etfal Training and Research Hospital
Responsible party
Mustafa Altınay (associate professor, Sisli Hamidiye Etfal Training and Research Hospital) — Principal investigator
First posted
Mar 20, 2025
Start date
Jun 1, 2024
Primary completion
Nov 1, 2025
Completion
Dec 1, 2025
Last update
Jan 21, 2026

Study contacts

AYSE SURHAN CINAR
study chair · şişli etfal eğitim araştırma hastanesi

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion