Skip to content

Improving Continuous Renal Replacement Therapy Outcomes in Neonates and Infants Through Interdisciplinary Collaboration

Improving Continuous Renal Replacement Therapy (CCRT) Outcomes in Neonates and Infants Through Interdisciplinary Collaboration

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05161078
Acronym
ICONIIC
Enrollment
1000
Registered
2021-12-16
Start date
2021-12-16
Completion date
2031-12-31
Last updated
2026-03-23

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

Conditions

Acute Kidney Injury, Chronic Kidney Diseases, Renal Dialysis

Brief summary

To date, little knowledge exists related to the use of hemodialysis (HD) in infants and has been limited to mainly single center studies. The CARPEDIEM (CArdio-Renal PEdiatric Dialysis Emergency Machine) device, which can be used to provide hemodialysis in infants, has been launched in the United States. This study/registry is designed to obtain data on critically ill infants who require HD using the CARPEDIEM device to understand the indications for initiation, best practice in prescribing and performing treatment, expected treatment course, and outcomes of a dedicated infant continuous renal replacement therapy (CRRT) machine.

Detailed description

This is a retrospective and prospective, multicenter observational quality improvement study and research registry. Infants undergoing renal replacement therapy utilizing CARPEDIEM for hemodialysis will be enrolled in the study for observation. There are two arms to this study, one for quality improvement and one for research purposes. Patients enrolled in this study have the option to participate additionally in either biospecimen collection, long term follow up after CARPEDIEM, or both. Urine specimen will be collected from fresh voids, but all blood specimen will be obtained from residual clinical specimen. Investigators hope to gain more information into use, treatment course, and outcomes from infants requiring treatment with the CARPEDIEM device.

Interventions

DEVICECARPEDIEM

CARPEDIEM treatment as per local standard of care

Sponsors

Children's Hospital Medical Center, Cincinnati
Lead SponsorOTHER
Mozarc Medical US LLC
CollaboratorINDUSTRY

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Treated with CARPEDIEM as part of standard of care at a participating institution within the United States

Exclusion criteria

* Parents/legally authorized representative unable or unwilling to provide consent

Design outcomes

Primary

MeasureTime frameDescription
Number of CARPEDIEM filters to meet prescribed treatment length24 hoursComparing actual time of treatment of each CARPEDIEM filter to the initial prescribed length of treatment at the time of filter initiation
Rate of patient survivalthrough hospital discharge, an average of less than 1 yearPercent of patients treated with the CARPEDIEM who survive to hospital discharge
Rate of renal recoverythrough hospital discharge, an average of less than 1 yearExcluding patients with End Stage Renal Disease (ESRD), percent of patients treated with the CARPEDIEM who recover baseline renal function as measured by liberation from dialysis and serum creatinine returning to within less than a 50% increase over baseline.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORCara Slagle, MD

Cincinnati Children's

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026