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New Short-Course malaria treatment could prevent relapse

NCT ID NCT05874271

First seen Nov 21, 2025 · Last updated Jun 19, 2026 · Updated 22 times

Summary

This study tested a new way to treat vivax malaria, a type that can hide in the liver and come back. Researchers gave patients a quick G6PD test to check for a genetic condition that can cause dangerous side effects from the drug primaquine. Then they used a high-dose, short-course primaquine regimen tailored to each patient's G6PD level. The goal was to see if this approach is safe, practical, and helps patients complete treatment. Over 790 people with vivax malaria took part in health centers in Papua New Guinea.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Baro Clinic

    Vanimo, Sandaun Province, Papua New Guinea

  • Mugil Health Centre

    Madang, Madang Province, Papua New Guinea

  • Napapar Health Centre

    Kokopo, East New Britain Province, Papua New Guinea

  • Wirui Clinic

    Wewak, East Sepik Province, Papua New Guinea

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

primaquine

What this could lead to

If successful, this approach could make radical cure of vivax malaria safer and more practical, reducing relapse rates in endemic areas.

What could go wrong

The study is a feasibility trial, not a large efficacy trial, so results may not confirm long-term benefits. Risks include haemolysis in G6PD-deficient patients despite testing.

Conditions

The condition(s) this trial relates to.

G6PD deficiency Plasmodium vivax malaria

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.