Hemodynamic Stability in Septic Shock Patients Undergoing Continuous Renal Replacement Therapy With oXiris Membrane

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSeoul National University Hospital

About this trial

The new adsorbing membrane for continuous renal replacement therapy (CRRT), oXiris, can reduce plasma cytokines and endotoxins in septic shock patients with severe acute kidney injury, compared with standard membranes. However, its hemodynamic stability or benefits have not been thoroughly evaluated although this is reasonable.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged ≥ 18 years

Sepsis related acute kidney injury requiring continuous renal replacement therapy

Disqualifiers

None

Trial population

Adult patients who have severe acute kidney injury and require continuous renal replacement therapy because of hemodynamic instability.

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • oXiris membrane

    Device

    Perform continuous renal replacement therapy with oXiris membrane

  • Polysulfone membrane

    Device

    Perform continuous renal replacement therapy with polysulfone membrane

Treatment groups

98 Participants
are divided into 1 treatment group
Group A: Septic AKI2 interventions

Trial outcomes

Primary outcomes

1

Rate of all-cause mortality

Risk of all-cause mortality

Time frame
28 days
2

Occurrence rates of ventricular tachycardia, intradialytic hypotension

Risk of ventricular tachycardia, intradialytic hypotension

Time frame
28 days

Secondary outcomes

Other outcomes

Sponsors and contacts

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