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NCT Number: NCT06989892

Comparing Super High-flux and High-flux Dialyzer Performance Among Hemodialysis Patient With Sepsis : a Randomized Control Trial

Comparing the efficacy of superhigh-flux dialyzer with high-flux dialyzer in ESKD patient who have sepsis to improve mortality and sepsis outcome, an open label randomized control trial.

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Key information

About this study

Sepsis in people who have ESKD is the risk of developing poor outcome. Cytokines play a role in the process of sepsis and cause the worsening clinical outcome despite definitive antibiotic treatment. Superhigh-flux dialyzer has a larger molecular weight cut off (MWCO) clearance, include cytokine, could contribute to improved sepsis management in individuals with ESKD. This study is conducted to prove the efficacy of super high-flux dialyzer comparing with high-flux dialyzer in case of mortality reduction for regular hemodialysis ESKD patients.

Method This study is an open label single center randomized control trial. We randomized ESKD patients who have sepsis condition with high interleukin-6 (IL-6 > 50 pg/ml).

The participants were allocated to super high-flux dialyzer group and high flux dialyzer group, stratified with diabetes, vascular access, and septic shock.

We excluded; patient who needed dialysis with continuous kidney replacement therapy, vulnerable patient, include pregnant woman, patient who closed and patient who expected to pass away within the 24 hours. We aim to enroll total 202 participants; divided equally in each arm. According to our protocol, non reused super high-flux dialyzer and high-flux dialyzer are used in the same assigned patient in first week without crossing over. The standard of care of sepsis and antibiotic are provided in both groups without intervening of researcher and our protocol. The primary endpoint is 28 days of mortality. The secondary outcome include cardiovascular death, rate reduction of IL-6 after dialysis, days of hospitalization, ventilator free days and complication of dialysis are also monitored.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ESKD patients who have sepsis condition with high interleukin-6 (IL-6 > 50 pg/ml)

Exclusion criteria

  • Patients who needed dialysis with continuous kidney replacement therapy, vulnerable patient, include pregnant woman, patient who expected to pass away within the 24 hours.
  • Patients who have the history of allergic dialyzer reaction to dialyzer which used in this trial.

Treatment and study plan

Super High-flux dialyzer (Elisio 19HDx)

Device

Dialysis with Super High-flux dialyzer for intervention group

High-flux dialyzer (Elisio 19H)

Device

Dialysis with High-flux dialyzer for control group

Primary outcomes

  1. Comparing the reduction of all cause death at 28 days

    Time frame: 28 days

    Comparing the efficacy to reduce all cause death at 28 days between Super High-flux dialyzer with High-flux dialyzer in ESKD with sepsis

Secondary outcomes

  1. Comparing the difference of blood level of IL-6, ESR, CRP and albumin, before and after of the first dialysis session, in each group.

    Time frame: 7 days

  2. The duration of inotrope weaning

    Time frame: 14 days

  3. The duration of hospitalization

    Time frame: 28 days

  4. Ventilator free days

    Time frame: 28 days

  5. The incidence of intradialytic hypotension

    Time frame: 28 days

  6. The incidence rate of complication of dialyzer in each group

    Time frame: 28 days

    The incidence rate of complication of dialyzer; allergic reaction, clotting of dialyzer etc.

  7. The adequacy profile of dialysis in both groups

    Time frame: 7 days

Study contacts

Contact information is provided by the study sponsor or research team.

Punnawit Laungchuaychok, MD

CONTACT

[email protected]

022443000

Wanjak Pongsittisak, MD

CONTACT

[email protected]

022443000

Sponsors and collaborators

Lead sponsor

Navamindradhiraj University

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
May 25, 2025
Registry last updated
May 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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