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Study identifier: NCT07267169 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efferon LPS Hemoadsorption in Patients With Acute Pancreatitis

Condition: Pancreatitis, Acute  ·  Sponsor: Efferon JSC

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

The goal of the study is to evaluate the safety and efficacy of multimodal (cytokine and lipopolysaccharide) hemoperfusion using the Efferon® LPS device in combination with hemofiltration (HF) / hemodiafiltration (HDF), with the goal of reducing the severity of organ dysfunction (measured by SOFA score) in patients with acute pancreatitis. Participants will be assigned to two groups for comparison: a control group receiving baseline therapy with HF/HDF, and a treatment group receiving baseline therapy in combination with HF/HDF and Efferon® LPS hemoadsorption.The therapy will be initiated within the first 24 hours after ICU admission and within 8 hours after patient enrollment.

This description comes directly from the study's public registry record.

Talk to the study team

Alexandr Shelehov-Kravchenko, PhD, MD  ·  +79636564765  ·  alexandr.shelehov@gmail.com

Always discuss trial participation with your own doctor first.

Locations (8)

Republican Clinical Hospital of the Ministry of Health of the Republic of TatarstanKazan', RussiaRecruiting
State Clinical Hospital "Regional Clinical Hospital No 2" of the Ministry of Healthcare of Krasnodar TerritoryKrasnodar, RussiaRecruiting
V.P. Demikhov City Clinical Hospital No. 68Moscow, RussiaRecruiting
S.S. Yudin City Clinical HospitalMoscow, RussiaRecruiting
N.I. Pirogov City Clinical Hospital No. 1Moscow, RussiaRecruiting
N.V. Sklifosovsky Research Institute for Emergency MedicineMoscow, RussiaRecruiting
Perm regional clinical hospitalPerm, RussiaRecruiting
North-Western district scientific and clinical center named after L. G. Sokolov Federal Medical and Biological AgencySaint Petersburg, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07267169