Can we unmask the hidden interference in filariasis testing?
NCT ID NCT04258670
First seen Aug 21, 2026 · Last updated Aug 21, 2026
Summary
This study investigates why people with loiasis, a parasitic infection, may test positive on rapid diagnostic tests for lymphatic filariasis. Researchers will follow 60 individuals with high loiasis worm burdens to monitor the release of filarial antigens in their blood. By identifying these cross-reactive proteins, the study aims to improve the accuracy of diagnostic tests for lymphatic filariasis.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could identify specific biomarkers to improve diagnostic tests, reducing false positives for lymphatic filariasis in regions where loiasis is common.
- What could go wrong
- This is an observational study with a small sample size, and findings may not generalize to all populations. The cross-reactive antigens may vary over time, complicating biomarker identification.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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86 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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May 2021
- 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
The study will be conducted in the Okola health district (Lékié Division, Centre Region, Cameroon), situated about 40km northeast of Yaoundé, the political capital city of Cameroon. The Okola health district is highly endemic for loiasis. Participant will be recruited among those excluded from an Onchocerciasis study due to high Mf counts \>20,000/mL.
- 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: * Ability to give informed consent * Loiasis Mf count \> 20,000 Mf/mL * Resident of study area * No evidence of severe or systemic comorbidities * Consent to storage of blood samples for future study Exclusion Criteria: * Subject plans to move from the study area during subsequent 12 months
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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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Centre for Research on Filariasis and other Tropical Diseases (CRFilMT)
Yaoundé, Cameroon
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