ClinicalTrials.Veeva

Menu

Cytokine Hemadsorption in Covid 19 Patients With Bacterial Sepsis

D

Derince Training and Research Hospital

Status

Unknown

Conditions

INTERLEUKIN 6

Treatments

Device: cytokine hemadsorption

Study type

Observational

Funder types

Other

Identifiers

NCT04920851
BIRUNI 1

Details and patient eligibility

About

In this retrospective study, we aimed to compare the laboratory and clinical results of cytokine hemadsorption as an immunomodulation therapy in COVID-19 ICU patients with or without sepsis.

Enrollment

23 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • COVID-19 patients were the available data of laboratory diagnosis of COVID-19 (a positive throat swab nucleic acid test or positive serum COVID-19 specific antibody test),
  • patients with COVID-19 induced sepsis was detection of bacterial agent in blood or tracheal culture

Exclusion criteria

  • below 18 aged
  • those who did not undergo hemoperfusion

Trial design

23 participants in 2 patient groups

Covid with sepsis
Description:
Covid patient with sepsis
Treatment:
Device: cytokine hemadsorption
covid without sepsis
Description:
Covid patient without sepsis
Treatment:
Device: cytokine hemadsorption

Trial contacts and locations

1

Loading...

Central trial contact

ilke küpeli

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems