Could a Finger-Prick test replace blood draws for kidney patients?
NCT ID NCT07777523
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This study evaluates a portable digital test called KF4+ that measures urea and potassium from a tiny drop of capillary blood, like a finger prick. The trial involves 55 adults with end-stage kidney disease who are on dialysis. The goal is to see if the KF4+ results match standard hospital lab tests done on venous blood, and whether it can also help assess dialysis efficiency. If it works, this could make routine monitoring easier and less invasive for patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- KF4+ noninvasive digital test for measuring urea and potassium in capillary blood
- What this could lead to
- If successful, this could enable simpler, more convenient monitoring of kidney dialysis patients, potentially reducing the need for frequent venous blood draws.
- What could go wrong
- This is a small observational study, and the test's accuracy compared to standard lab methods is not yet proven. It may not be reliable enough for routine clinical use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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55 people
The number who actually took part.
- Started
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Oct 2025
- Finished
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Dec 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
End-Stage Chronic Kidney Disease Patients under Chronic Dialysis from Hospital Interzonal General de Agudos General San Martín La Plata, Argentina
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patients (≥18 years) * Diagnosis of end-stage renal disease * Receiving chronic dialysis treatment * Receiving chronic hemodialysis treatment * Able and willing to provide written informed consent Exclusion Criteria: * Inability to provide informed consent * Any condition that, in the opinion of the investigator, would interfere with participation or data interpretation
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Hospital Interzonal General de Agudos General San Martín La Plata, Argentina
La Plata, Buenos Aires, 1900, Argentina
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Other studies related to the condition(s) this trial covers.
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