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A randomised, open comparative study of Dihydroartemisinin-piperaquine versus Chloroquine for the treatment of Vivax malaria

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN87827353
Enrollment
500
Registered
2006-08-08
Start date
2006-08-15
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Uncomplicated vivax malaria Infections and Infestations Uncomplicated vivax malaria

Interventions

Dihydroartemisinin-piperaquine versus Chloroquine treatment.

Sponsors

University of Oxford (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Males and Females aged over 12 months 2. Body weight more 5 kg 3. Microscopically confirmed, mono-infection of Plasmodium vivax (parasitaemia more than or equal to 5/500 White Blood Cells [WBC]) 4. Fever (axillary temperature more than or equal to 37.5°C) OR history of fever 5. Informed consent obtained by patients and in the case of children, by parents or guardians 6. Willingness and ability to comply with the study protocol

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to the study drugs 2. Presence of intercurrent illness or any condition which in the judgement of the investigator would place the subject at undue risk or interfere with the results of the study 3. Pregnancy or lactation, urine test for beta human Chorionic Gonadotropin (beta-hCG) to be performed on any woman of child bearing age 4. Mefloquine treatment in the previous 60 days 5. Dapsone Pyrimethamine (DP) treatment in the previous three months

Design outcomes

Primary

MeasureTime frame
Day 63 cure

Secondary

MeasureTime frame
Safety

Countries

Thailand

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026