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Effect of Cytosorb on Blood Levels of Inflammatory Biomarkers of Sepsis.

U

University of Gaziantep

Status

Completed

Conditions

Cytokine Storm
Sepsis

Treatments

Device: Cytokine aphaeresis

Study type

Observational

Funder types

Other

Identifiers

NCT04226430
TF.18.43

Details and patient eligibility

About

Background: There is still an evident need for useful biomarkers and effective therapeutic approaches regarding the challenging management of sepsis. The aim of the study is to evaluate the effect of each Cytosorb hemoadsorption therapy course on blood levels of inflammatory biomarkers of sepsis including endocan, copeptin, interleukin-6, procalcitonin, C-reactive protein.

Full description

This observational prospective study included patients, who were diagnosed with sepsis and treated in the reanimation ICU of Gaziantep University Hospital with Cytosorb therapy between June 1st, 2016 and June 30th, 2017. Sepsis was diagnosed according to The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3).

Exclusion criteria of the study were: (i) cardiovascular disease, (ii) multiple traumas, (iii) malignancies, (v) incomplete clinical data.

Approval of the ethical committee (ethical committee approval number 2018/04-02) was obtained. Written informed consent was taken from each patient or their next-of-kin. Patient demographics including age, gender, and origin of sepsis were recorded. Arterial blood samples were taken from patients before and immediately after the Cytosorb therapy course.

Enrollment

34 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients, who were diagnosed with sepsis and treated in the reanimation ICU of Gaziantep University Hospital with Cytosorb therapy (Sepsis was diagnosed according to The Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3))

Exclusion criteria

  • cardiovascular disease,
  • multiple traumas
  • malignancies
  • incomplete clinical data.

Trial design

34 participants in 2 patient groups

Before cytosorb
Description:
Arterial blood samples were taken from patients before the Cytosorb therapy course.
Treatment:
Device: Cytokine aphaeresis
after cytosorb
Description:
Arterial blood samples were taken from patients immediately after the Cytosorb therapy course.
Treatment:
Device: Cytokine aphaeresis

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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