Can a simple preventive drug cut malaria and anemia in infants?
NCT ID NCT05889052
First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time
Summary
This trial tests whether giving infants a preventive dose of the antimalarial drug sulfadoxine-pyrimethamine during routine health visits can lower their risk of malaria and anemia. Researchers will follow about 2,100 children in Cameroon, comparing those in areas receiving this preventive care with those receiving standard care. The study tracks malaria infections, anemia, and severe outcomes over 18 months to see if this approach works in real-world settings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sulfadoxine-pyrimethamine, an antimalarial drug given as preventive treatment to infants
- What this could lead to
- If effective, this could support routine malaria prevention in infants, reducing malaria cases, severe anemia, and deaths in young children.
- What could go wrong
- The trial is still in progress, and results may not show a clear benefit. The drug may also have side effects or face resistance in some areas.
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
-
2,138 people
The number who actually took part.
- Started
-
Jul 2023
- Finished
-
Dec 2025
- Lead sponsor
-
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
Children up to 9 months of age in Soa and Mbankomo health districts of Cameroon.
- Ages
-
Up to 9 months
- Sex
-
Anyone
- Healthy volunteers
-
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: * Reside in Soa (intervention) or Mbankomo (control) health districts. * Agree to take part in the census. * Aged 6-9 months at the time of enrolment. Exclusion Criteria: * Parent/caregiver refused to participate in the cohort. * Parent/caregiver did not give informed consent.
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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
-
Multiple
Soa and Mbankomo, Cameroon
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Other studies related to the condition(s) this trial covers.
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