Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07293936

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients initiated on continuous renal replacement therapy (CRRT)
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Patients currently receiving extracorporeal membrane oxygenation (ECMO) treatment

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Measurement Procedure

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

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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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