NCT06404424

Combined Hemoperfusion and Therapeutic Plasma Exchange for Treatment of Patients With Septic Shock

Consecutive Hemoperfusion and Therapeutic Plasma Exchange in Adult Patients With Septic Shock
Efferon JSC·ClinicalTrials.gov·device·Device trialCompleted
View on ClinicalTrials.gov
Study focus
Disease/Condition
Sepsis,Septic Shock
Drug/Device/Intervention
Efferon LPS
Study type
Observational
Intervention type
device
Sponsor & location
Primary sponsor
Efferon JSC
Location
Moscow, Russian Federation
Timeline & enrollment
Phase
N/A
Start date
May 01, 2022
End date
Mar 01, 2024
Enrollment
82 participants
Primary outcome

Shock - Free Days

Summary

Sepsis is a critical burden for a healthcare. From 2000 to 2020, the number of publications
 and clinical studies on the topic of Sepsis and septic shock on the National Library of
 Medicine resource The National Center for Biotechnology Information has tripled. Sepsis is a
 life-threatening condition that causes significant pathophysiological changes in the body.
 Currently, sepsis is understood as organ dysfunction caused by a dysregulatory response of
 the macroorganism to infection. A special role in this process belongs to the innate and
 adaptive immune response.
 
 Despite the trend towards improving survival rates, mortality in sepsis remains high - about
 25%, reaching 60% with the development of septic shock.
 
 Extracorporeal therapy, as an adjuvant method of treatment, has been used for more than 30
 years, but conducting large randomized studies confirming its effectiveness is associated
 with a complex of problems, including the extreme heterogeneity of the population of patients
 with sepsis and septic shock, different etiologies and complex pathogenesis, non-identical
 pathophysiological pathways of the dominant organ dysfunction in specific time period and
 degree of its severity.
 
 Goal of the study is to evaluate safety and efficiency of combined hemoperfusion and
 therapeutic plasma exchange in adult patients with septic shock.

ICD-10 classifications
Septic shockOther sepsisOther specified sepsisSepsis, unspecifiedSepsis due to other specified staphylococcus
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06404424
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT06404424 through Pure Global AI's free database. This phase not specified trial is sponsored by Efferon JSC and is currently Completed. The study focuses on Sepsis,Septic Shock. Target enrollment is 82 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.