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HFR Cartridge and Inflammation

F

Federico II University

Status

Completed

Conditions

P-cresol
Inflammatory Status

Treatments

Procedure: HFR dialysis

Study type

Interventional

Funder types

Other

Identifiers

NCT01865773
HFRinflamm
HFR13

Details and patient eligibility

About

A major limitation of standard hemodialysis is that it does not clear the plasma from interleukin-6 (IL-6) and p-cresol, two uremic toxins responsible for the high cardiovascular risk in end stage renal disease (ESRD). In the present study, we evaluated whether these compounds are removed by HFR-Supra, a double-chamber hemodiafiltration system in which the ultrafiltrate (UF) returns to the patient after its regeneration through a resin cartridge. We selected 8 inflamed chronic hemodialysis (HD) patients, which underwent a single 240 minutes HFR session. We studied the change in both IL-6 and p-cresol circulating levels, by comparing pre- and post-HFR serum concentrations. In addition, we compared Il-6 and p-cresol levels in the UF entering (UFin) and exiting (UFout) from the cartridge, either at the start or at the end of the HFR session. The proinflammatory activity of UFin and UFout was determined by evaluating the changes that they induced in IL-6 messenger ribonucleic acid (mRNA) expression and release in peripheral blood mononuclear cells (PBMC) collected from 8 healthy volunteers and cultured in vitro for 24 hr.

Enrollment

8 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • HD patients undergoing three weekly haemodialysis > 1 year

Exclusion criteria

  • none

Trial design

8 participants in 1 patient group

HFR
Experimental group
Description:
We selected 8 inflamed chronic HD patients, which underwent a single 240 minutes HFR session
Treatment:
Procedure: HFR dialysis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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