Retrospective Analysis of Prismaflex HF20 Set Versus ppCRRT Registry

Description

A retrospective multicenter, observational design intended to capture data on pediatrics (weighing between 8 - 20 kg) who underwent continuous renal replacement therapy (CRRT) using the HF20 set. Data will be compared with a similar population (weighting 8-20 kg) from the ppCRRT registry who received CRRT with Prismaflex M60 sets.

Conditions

Acute Renal Failure (ARF), Acute Kidney Injury (AKI), Fluid Overload in Dialysis Patients

Study Overview

Study Details

Study overview

A retrospective multicenter, observational design intended to capture data on pediatrics (weighing between 8 - 20 kg) who underwent continuous renal replacement therapy (CRRT) using the HF20 set. Data will be compared with a similar population (weighting 8-20 kg) from the ppCRRT registry who received CRRT with Prismaflex M60 sets.

Comparison of Patient Outcomes Between Retrospective Prismaflex HF20 Set and Historical Prospective Pediatric Continuous Renal Replacement Therapy (ppCRRT) Registry

Retrospective Analysis of Prismaflex HF20 Set Versus ppCRRT Registry

Condition
Acute Renal Failure (ARF)
Intervention / Treatment

-

Contacts and Locations

Palo Alto

Lucile Packard Children's Hospital Stanford, Palo Alto, California, United States, 94304

Aurora

Children's Hospital Colorado, Aurora, Colorado, United States, 80920

Chicago

Ann and Robert H Lurie Children's Hospital of Chicago, Chicago, Illinois, United States, 60611

Cincinnati

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States, 45229

Dallas

Children's Medical Center of Dallas, Dallas, Texas, United States, 75235

Seattle

Seattle Children's Hospital Research and Foundation, Seattle, Washington, United States, 98105

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Patient weighed between 8 and 20 kg (17.6 - 44.1 lb).
  • 2. Patient received medical care in an intensive care unit (ICU) and was treated with HF20 based CRRT.
  • 3. Patient had a clinical diagnosis of AKI or ARF or fluid overload requiring CRRT.

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Baxter Healthcare Corporation,

Study Record Dates

2025-05