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Clinical Trials in Turkey / NCT06808100
Enrolling by invitation Observational

Can Gdf-15 Level Predict Progression to Multiple Organ Failure in Patients With Septic Shock

NCT06808100 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-05-01
Last updated
2025-07-28

Condition(s) studied

SepsisSeptic ShockMulti Organ Failure

Study summary

The aim of this observational study is to investigate whether GDF-15 levels can predict clinical outcome in patients admitted to the intensive care unit with a diagnosis of septic shock.

The main question is:

* Can the level of GDF-15 levels during ICU admission predict the development of multiple organ failure in patients with septic shock? All patients will continue to receive routine treatment for sepsis and septic shock. The investigators will observe the development of multiple organ failure by the Sequential Organ Failure Assessment (SOFA) score increase

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients older thab 18 years of age * Patients with septic shock * Patients without end-stage renal failure (KDIGO G4,G5) * Patients without chronic liver disease * Patients with New York Heart Association (NYHA) stage 1-2 * Patients not diagnosed with active cancer * Non-pregnant patients * Patients without chronic immunodeficiency * Patients without chronic inflammatory disease Exclusion Criteria: * Patients younger than 18 years age * Patients not diagnosed with septic shock * Patients with end-stage renal failure * Patients with chronic liver disease * Patients with New York Heart Association (NYHA) stage 3-4 * Patients diagnosed with active cancer * Pregnant patients * Patients with chronic immunodeficiency * Patients with chronic inflammatory diseases

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ankara Bilkent City Hospital Ankara Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06808100 on ClinicalTrials.gov ↗ ← All trials in Turkey