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| Name | Class |
|---|---|
| Institute of Tropical Medicine, Belgium | OTHER |
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Several countries in Africa have changed their first-line treatment for uncomplicated malaria to an ACT. Burkina Faso has changed its policy to Artemether-Lumefantrine (AL) and Artesunate-Amodiaquine (AQ+AS). However, such choice has been done without knowing the local effectiveness of these drugs when they are given to patients in real life conditions, without direct observation of the drug administration. Thus, this study aims at investigating the effectiveness of AQ+AS and AL, when given to children with uncomplicated malaria in Burkina Faso.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Artemether -lumefantrine | Experimental | Experimental Treatment of malaria with Artemether-lumefantrine (AL), according to one of the two options given by national protocol in Burkina Faso |
|
| Artesunate-amodiaquine | Experimental | Treatment of malaria with Artesunate-amodiaquine(AS-AQ), according to one of the two options given by national protocol in Burkina Faso |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Artesunate-amodiaquine | Drug | Coformulated AQ+AS by Sanofi-Aventis has been pre-qualified by WHO in 2008. It is administered once daily for three consecutive days, and it is available in three different dosages (25mg/67.5mg; 50mg/135mg; 100mg/270mg) |
| Measure | Description | Time Frame |
|---|---|---|
| Polymerase chain reaction (PCR) adjusted treatment failure | Day 28 |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment failure up to day 42 (PCR adjusted and unadjusted) | Day 42 | |
| Gametocytes (prevalence and density) | At day 7, 14, 21, 28, 35 and 42 days after treatment | |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Nanoro | Nanoro | Boulkiemdé | 115 | Burkina Faso | ||
| Nanoro |
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|
| Artemether-lumefantrine | Drug | Artemether-lumefantrine by Novartis was the first fixed-dose ACT that was prequalified by WHO in April 2004. A 3-day, 6-dose regimen of AL is recommended for infants and children weighing 5-35 kg and adults weighing > 35 kg. |
|
|
| Hb changes |
| Day 35 |
| Nanoro |
| Boulkiemdé |
| Burkina Faso |
| IRSS-DRO/Centre Muraz | Bobo-Dioulasso | Bp 545 | 01 | Burkina Faso |
| Tinto Halidou | Bobo-Dioulasso | Houet | 01 | Burkina Faso |
| ID | Term |
|---|---|
| C515299 | amodiaquine, artesunate drug combination |
| D000077611 | Artemether, Lumefantrine Drug Combination |
| ID | Term |
|---|---|
| D000077549 | Artemether |
| D037621 | Artemisinins |
| D017382 | Reactive Oxygen Species |
| D005609 | Free Radicals |
| D007287 | Inorganic Chemicals |
| D009930 | Organic Chemicals |
| D000078102 | Lumefantrine |
| D005449 | Fluorenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D012717 | Sesquiterpenes |
| D013729 | Terpenes |
| D011083 | Polycyclic Compounds |
| D004338 | Drug Combinations |
| D004364 | Pharmaceutical Preparations |
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