Lipopolysaccharide Adsorption (Efferon LPS NEO) in Children With Thermal Burns
Recruiting
Observational Study
Burns
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 1 – 14
- Sex
- Any
- Study type
- Observational
- Participants needed
- 30 (estimated)
- Sponsor
- Efferon JSC · Industry
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Thermal burn of Ⅱ and Ⅲ severity with a lesion area of 40% or more (ICD-10: T20-T25, T29)
* Frank index \>90 (Frank Index quantifies burn severity based on the depth and total surface area of the skin lesion)
* Start of hemoadsorption no later than 5 days after admission to th…
Contacts