Assessment of an Anemia Model Predictive Controller for Anemia Management in Hemodialysis Patients

Status unconfirmed · Not applicable

Conditions studied: End Stage Renal Disease, Renal Anemia, Chronic Kidney Diseases

In brief

The purpose of this randomized, controlled pilot study is to evaluate the performance of this novel Anemia Controller (vis-à-vis standard of care) for anemia management in hemodialysis patients. Since the Anemia Controller is designed to bring patients to a pre-defined Hgb target level and keep them there, the target population for this study are patients whose Hgb levels are currently not well-controlled (rather than patients who are already relatively stable within the Hgb target range under a standard anemia management algorithm). Specifically, therefore, the target population for this clinical study are chronic hemodialysis patients who are exhibiting Hgb cycling.

Key facts

Study ID

NCT04360902

Run by

Renal Research Institute

People needed

60

Starts

2020-01-08

Expected to finish

2021-12-01

Last updated by the study team

2020-04-24

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥18 years
• Ability to give written informed consent to the study
• End-stage renal disease treated with thrice-weekly hemodialysis for at least 180 days preceding enrollment
• Receiving intradialytic Crit-Line® monitoring, with available Crit-Line® data going back at least 180 days from the date of enrollment
• Laboratory Hgb data going back at least 180 days from the date of enrollment
• On average, Hgb values available from at least 2 treatments per week (from either source, Crit-Line® or laboratory) during the past 180 days preceding enrollment
• Renal anemia treated with intravenous Mircera®, with at least 2 Mircera® dose administrations during the 150 days preceding enrollment
• On an active Mircera® anemia management algorithm order during the 180 days preceding enrollment
• Exclusively on Mircera® (no other ESAs) during the 180 days preceding enrollment
• Pattern of Hgb cycling as defined above during the 180 days preceding enrollment

You may not qualify if…

• Having received the maximum Mircera® dose (225 µg every other week) consistently throughout the 90 days preceding enrollment
• Hospitalization for more than 10 days during the 30 days preceding enrollment
• Severe iron deficiency (TSAT <20%, ferritin <100 ng/mL) in the most recent routine blood work prior to enrollment
• Any known cause of ESA resistance other than iron deficiency and inflammatory states (e.g. hematologic malignancies, hypersplenism, antibody mediated pure red cell aplasia)
• Simultaneous participation in another clinical study that may impact anemia management or the outcomes of this trial
• Inability to communicate in English or Spanish

Where it is running

• RRI — New York, New York, United States (enrolling)

Full record on ClinicalTrials.gov

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