Actively Recruiting
Validation of a Post-Filter Hematocrit Calculation Formula Compared to Measured Values in Continuous Renal Replacement Therapy Patients
Led by Gwyndolyn M. Radford · Updated on 2025-12-19
20
Participants Needed
1
Research Sites
6 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating a new formula to calculate post-filter hematocrit in patients undergoing continuous renal replacement therapy (CRRT). This study aims to validate whether the calculated post-filter hematocrit matches the values measured directly from blood samples. Filter clotting is a significant complication during CRRT, causing blood loss and treatment challenges, so finding accurate markers to predict clotting risk is important. Participants will have blood samples collected from their CRRT machine's post-filter lines at various times and flow rates. The study compares the hematocrit calculated by the formula HCTpost=HCTpre/(FF(HCTpre-1)+1) to measured hematocrit values from these samples. All participants receive the same procedure of both calculation and measurement. The study is cross-sectional, with participation lasting generally no longer than one day. During the study, four post-filter blood samples are collected over about 40 minutes. Researchers will analyze agreement between measured and calculated hematocrit and explore how CRRT settings and patient factors affect differences. There are no additional treatments or follow-up visits. Participation ends after the final blood draw, and safety monitoring is not specifically mentioned due to the short, observational nature of the procedure.
CONDITIONS
Brief Title
Post-Filter Hematocrit
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients initiated on continuous renal replacement therapy (CRRT)
- Age 18 years or older
You will not qualify if you...
- Patients currently receiving extracorporeal membrane oxygenation (ECMO) treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Less than 1 day
Participants undergo a single study procedure where four post-filter blood samples are collected over approximately 40 minutes to compare calculated and measured hematocrit values.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
University of Iowa Hospitals and Clinics
Iowa City, Iowa, United States, 52242
Actively Recruiting
Research Team
G
Gwyndolyn M Radford, MD
B
Benjamin R Griffin, MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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