RECRUITING

Retrospective Analysis of Prismaflex HF20 Set Versus ppCRRT Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2024-12-11
Study Completion:2025-05
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06633029

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.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patient weighed between 8 and 20 kg (17.6 - 44.1 lb).
  2. 2. Patient received medical care in an intensive care unit (ICU) and was treated with HF20 based CRRT.
  3. 3. Patient had a clinical diagnosis of AKI or ARF or fluid overload requiring CRRT.
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Baxter CORP Clinical Trials Disclosure
CONTACT
(224) 948-7359
Global_CORP_ClinicalTrialsDisclosure@baxter.com

Study Locations (Sites)

Lucile Packard Children's Hospital Stanford
Palo Alto, California, 94304
United States
Children's Hospital Colorado
Aurora, Colorado, 80920
United States
Ann and Robert H Lurie Children's Hospital of Chicago
Chicago, Illinois, 60611
United States
Cincinnati Children's Hospital Medical Center
Cincinnati, Ohio, 45229
United States
Children's Medical Center of Dallas
Dallas, Texas, 75235
United States
Seattle Children's Hospital Research and Foundation
Seattle, Washington, 98105
United States

Collaborators and Investigators

Sponsor: Baxter Healthcare Corporation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-12-11
Study Completion Date2025-05

Study Record Updates

Study Start Date2024-12-11
Study Completion Date2025-05

Terms related to this study

Keywords Provided by Researchers

  • Continuous Renal Replacement Therapy
  • CRRT

Additional Relevant MeSH Terms

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