Lipopolysaccharide Adsorption (Efferon LPS NEO) in Children With Thermal Burns

Recruiting now

Conditions studied: Burns

In brief

This observational pilot study aims to identify criteria for evaluating the effectiveness of hemoadsorption with the Efferon LPS NEO device in pediatric burn injury. Participants will be prospectively assigned to the treatment group and compared with a retrospectively selected control group. Each patient in the treatment group will undergo two hemoadsorption sessions, each lasting 6-12 hours, with an interval of 24-120 hours between procedures. The sessions may be performed in combination with hemofiltration or hemodiafiltration at the discretion of the investigator.

Key facts

Study ID
NCT07248930
Run by
Efferon JSC
People needed
30
Starts
2025-10-01
Expected to finish
2027-03-31
Last updated by the study team
2025-11-25

Who can join

Age: 1 and older, up to 14. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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