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Pilot Study: Comparison of the efficacy of artemisinin plus piperaquine (Artequick), artesunate plus amodiaquine (Coarsucam) and artesunate plus azithromycin for the treatment of Plasmodium falciparum malaria in Vietnam

Pilot Study: Comparison of the efficacy of artemisinin plus piperaquine (Artequick), artesunate plus amodiaquine (Coarsucam) and artesunate plus azithromycin for the treatment of Plasmodium falciparum malaria in Vietnam

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000816257
Enrollment
128
Registered
2009-09-18
Start date
2008-05-27
Completion date
2009-11-29
Last updated
2024-09-16

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

Conditions

None listed

Brief summary

Over 80 countries worldwide use artemisinin-based combination therapy (ACT) as first-line treatment of Plasmodium falciparum malaria. Debate continues as to the most effective ACT and how they will be deployed. Which ACT is the best combination therapy for first-line treatment in Vietnam has not been adequately studied. In the present study, we propose to investigate the efficacy and tolerability of three ACTs (artemisinin plus piperaquine, artesunate plus amodiaquine and artesunate plus azithromycin) in central Vietnam.

Interventions

Malaria patients will be administered either Artequick (2.5 mg/kg artemisinin and 15 mg/kg piperaquine daily) for 2 days, Coarsucam (4 mg/kg artesunate plus 10 mg/kg amodiaquine daily) for 3 days or 4 mg/kg artesunate plus 30 mg/kg azithromycin daily for 3 days. The mode of administration is oral dosing.

Sponsors

Australian Army Malaria Institute
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
5 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

(i) Sex: male or female (ii) Age: Between 5 years and 65 years old (iii) Falciparum malaria with parasitaemia between 200 and 200,000 parasites/uL of blood (iv) Is willing to give small amounts of blood via finger prick and phlebotomy (vi) Written informed consent and agreed to treatment follow-up for a total of 42 days

Exclusion criteria

(i) Severe/cerebral malaria or history of another serious medical disease (ii) Prior treatment with an artemisinin drug within the previous 7 days (iii) Pregnancy and lactating (iv) Inability to communicate well with the investigator (poor mental development or evidence of psychiatric disorder)

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 26, 2026