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Monitoring the efficacy and safety of Dihydro-Artémisinine-Piperaquine, Artemether-lumefantrine and Artesunate-Amodiaquine for malaria treatment

MONITORING THE EFFICACY AND THE SAFETY OF THREE ARTEMISININ COMBINATIONS THERAPIES (ACT) IN SENEGAL: RESULTS FROM TWO YEARS SURVEILLANCE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201305000552290
Enrollment
450
Registered
2013-05-15
Start date
2011-10-13
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Malaria

Interventions

Artesunate Amodiaquine (ASAQ)
Dehydroartemisinine Piperaquine (DHAPQ)

Sponsors

University Cheikh Anta DIOP of Dakar
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects aged over 6 months with the uncomplicated P. falciparum malaria, Parasite density between 1000 and 100000 trophozoites/¿l, Presence of an axillary temperature higher than 37.5° or history of fever during the previous 24 hours, Ability to take oral medication and given her inform consent were included in the study

Exclusion criteria

Exclusion criteria: Patients presenting mono-infestation by another species or mixted infestation, severe vomiting, severe malnutrition, severe signs of malaria (such as severe anemia, convulsion, respiratory distress), women with positive pregnancy test and patients who had a history of allergy to study drugs or not given her inform consent were excluded in the study

Design outcomes

Primary

MeasureTime frame
adequate clinical and parasitological response (ACPR) after corrected PCR at day 28

Secondary

MeasureTime frame
ACPR at days 35 and 42;Parasite and fever clearence time;Incidence of drug related adverse events

Countries

Senegal

Contacts

Public ContactMagatte NDiaye

Focal point of antimalarial drugs resistance in the department of Parasitology

magou22000@yahoo.fr00 221 77 609 11 07

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026