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Prospective observational study on cytokine removal in continuous hemodiafiltration

Prospective observational study on cytokine removal in continuous hemodiafiltration - Prospective observational study on cytokine removal in continuous hemodiafiltration

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040565
Enrollment
150
Registered
2020-05-28
Start date
2020-02-07
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients who started continuous hemodiafiltration

Interventions

None listed

Sponsors

Juntendo University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with written or verbal consent

Exclusion criteria

Exclusion criteria: Patients who the investigator determined to be inappropriate as subjects (Patients who deviate from the dialysis conditions [dialysis fluid 0.4 L / hour, replacement fluid 0.4 L / hour], who also use endotoxin adsorption therapy, who need to change the purification membrane within 24 hours of CHDF start, and within 24 hours. Those who have completed CHDF)

Design outcomes

Primary

MeasureTime frame
Changes in various blood cytokine levels 2, 18 and 24 hours after the start of CHDF

Countries

Japan

Contacts

Public ContactJunichiro Nakata

Juntendo University Hospital Department of Nephrology

jnakata@juntendo.ac.jp03-3813-3111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026