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Trials / Recruiting

RecruitingNCT07123909

Studies on Adsorption International Learning Initiative Global

The Use of Sorption Technologies in Patients Receiving Program Hemodialysis With Inflammatory Syndrome

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Botkin Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Use of sorption technologies in patients undergoing maintenance hemodialysis with inflammatory syndrome and clinical manifestations of uremia

Detailed description

This study will involve 30 hemodialysis patients selected based on examination results showing elevated C-reactive protein (CRP) and/or interleukin-6 (IL-6) levels. Participants will undergo hemoadsorption with the Jafron HA130 cartridge performed concurrently with hemodialysis: three times per week during the first month, twice per week during the second month, and once per week during the third month. The following parameters will be assessed: inflammatory markers (CRP, IL-1, IL-6, IL-8, β2-microglobulin, free light chains of immunoglobulins), parathyroid hormone (PTH), standard biochemical blood tests (creatinine, urea, calcium, phosphorus, albumin, iron metabolism), and complete blood count. Analyses will be performed at baseline (before inclusion) and monthly thereafter.

Conditions

Interventions

TypeNameDescription
DEVICEPatients will undergo a combined hemodialysis and hemosorption procedure. The study cartridge for hemosorption by Jafron HA130 contains the original adsorbing material.The test cartridge will be used in addition to the ongoing program hemodialysis three times a week in the first month, twice a week in the next month, once a week in the third month

Timeline

Start date
2025-06-01
Primary completion
2026-03-31
Completion
2026-06-30
First posted
2025-08-14
Last updated
2025-12-10

Locations

1 site across 1 country: Russia

Source: ClinicalTrials.gov record NCT07123909. Inclusion in this directory is not an endorsement.