Can a 15-Minute test stop a deadly virus in its tracks?
NCT ID NCT06894758
First seen Aug 27, 2026 · Last updated Aug 28, 2026 · Updated 1 time
Summary
This trial evaluates a new rapid diagnostic test designed to detect Crimean-Congo hemorrhagic fever (CCHF) at the point of care. The test aims to provide results in minutes instead of the current 2-5 days, which could speed up treatment and reduce the risk of the disease spreading. Researchers will test the device using 200 fresh blood samples from patients in Turkey during the 2025 CCHF season. If the test meets World Health Organization standards, a larger clinical trial will follow to support regulatory approval.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- A rapid diagnostic test (RDT) prototype that detects Crimean-Congo hemorrhagic fever viral antigens in blood samples.
- What this could lead to
- If the test proves accurate, it could enable fast, on-the-spot diagnosis of Crimean-Congo hemorrhagic fever, allowing earlier treatment and reducing the spread of the disease.
- What could go wrong
- The test is still in early development, and this study is relatively small. It may not meet the accuracy standards needed for regulatory approval, and its performance with fresh samples is still unproven.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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196 people
The number who actually took part.
- Started
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Jun 2025
- Finished
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Oct 2025
- 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.
Who is studied
Participants suspected of CCHF infection requiring a standard of care test.
- Ages
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18 years and older
- 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: 1. Willing to give whole blood samples (in a serum tube and EDTA tube) suspected of CCHF from Türkiye, Department of Infectious Diseases and Clinical Microbiology, Medical Faculty, Sivas Cumhuriyet University, Sivas or the department of Infectious Diseases or Ondokuz Mayis University (OMU) Faculty of Medicine, Department of Clinical Microbiology and Infectious Diseases, Samsun, that have not been frozen or refrigerated. 2. Adults aged 18 or over. Exclusion Criteria: None
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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
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Department of Infectious Diseases and Clinical Microbiology, Medical Faculty, Sivas Cumhuriyet University, Sivas
Sivas, 58000, Turkey (Türkiye)
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Ondokuz Mayis University (OMU) Faculty of Medicine, Department of Clinical Microbiology and Infectious Diseases, Samsun
Samsun, 55200, Turkey (Türkiye)
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