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EFFECTS OF EXTRACORPOREAL CYTOKINE ELIMINATION ON HEMODYNAMIA AND MORTALITY IN CRITICAL PATIENTS

EFFECTS OF EXTRACORPOREAL CYTOKINE ELIMINATION ON HEMODYNAMIA AND MORTALITY IN CRITICAL PATIENTS

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05984407
Enrollment
30
Registered
2023-08-09
Start date
2023-08-01
Completion date
2024-02-01
Last updated
2023-08-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cytokine Hemadsorption Therapy in Critically Ill Patients Who Have no Microbiological Findings and Develop Vasoplegic Shock

Keywords

vasoplegic shock, cytokine hemadsorption, hemodynamics, mortality, cytokine storm

Brief summary

Observation of the effects of cytokine adsorbent hemadsorption therapy on hemodynamics and mortality in critically ill patients who developed vasoplegic shock due to hyperinflammation without microbiological findings in the intensive care unit.

Detailed description

Observation of the effects of cytokine adsorbent hemadsorption therapy on hemodynamics and mortality in critically ill patients who developed vasoplegic shock due to hyperinflammation without microbiological findings and met the inclusion criteria in the Intensive Care Unit between 01.08.2023 and 01.02.2024

Interventions

PROCEDUREcytokine hemadsorption therapy

Observation of cytokine hemadsorption therapy in critically ill patients who have no microbiological findings and develop vasoplegic shock.

Sponsors

Hakan Küçükkepeci
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* C-reactive protein (CRP) ≥ 100 mg/l * Procalcitonin (PCT) \< 2 ng/l * Patients aged 18-80 years who were treated with cytokine adsorption due to vasoplegic shock

Exclusion criteria

* Patients under 18 years of age * Patients with suspected or proven bacterial cause of vasoplegic shock. * Those who did not approve to participate in the study * Patients without vasoplegic shock * Patients with CRP \< 100 mg/l, PCT ≥ 2 μg/L

Design outcomes

Primary

MeasureTime frame
The time to resolution of vasoplegic shock within days.From enrollment to the end of treatment at 12 weeks

Secondary

MeasureTime frame
Interleukin 1 beta level on day 1one day
Interleukin 10 level on day 1one day
Interleukin 6 level on day 1one day
TNF - α level on day 1one day
Interleukin 1 beta level on day 33 days
7-day mortality7 days
mortality until discharge from hospitalFrom enrollment to the end of treatment at 12 weeks
Interleukin 6 level on day 33 days
TNF - α level on day 33 days
mechanical ventilation need and durationFrom enrollment to the end of treatment at 12 weeks
duration of treatment in the intensive care unitFrom enrollment to the end of treatment at 12 weeks
dose of catecholamineFrom enrollment to the end of treatment at 12 weeks
Interleukin 10 level on day 33 days

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026