New finger prick test could spot toxoplasma infection in minutes
NCT ID NCT04474132
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study is testing a new finger prick device that can detect Toxoplasma infection from a drop of blood. Researchers will compare the device's results to a standard lab test in 210 adults, including pregnant women. The goal is to see if the finger prick test is accurate and easy to use, which could make testing faster and more convenient.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Toxoplasma ICT IgG-IgM BK finger prick test device
- What this could lead to
- If successful, this could provide a quick, easy finger prick test for Toxoplasma infection, making diagnosis more accessible.
- What could go wrong
- This is an early feasibility study with only 210 participants. The new test may not match the accuracy of the standard lab test, and results may not apply to all populations.
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.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 210 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2020
- Expected to finish
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Aug 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * any adult who is willing to participate in the study Exclusion Criteria: * pregnant women who are in their 17-27 weeks of gestation.
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Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Chicago
RECRUITINGChicago, Illinois, 60637, United States