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| Name | Class |
|---|---|
| World Health Organization | OTHER |
| Medical Research Council, South Africa | OTHER |
| Global Fund | OTHER |
The purpose of this study is to compare the efficacy of sulfadoxine-pyrimethamine plus artesunate with that of sulfadoxine-pyrimethamine on its own for the treatment of uncomplicated malaria.
Resistance of Plasmodium falciparum to anti-malarial drugs is a serious impediment to malaria control. In the South East African Combination Anti-malarial Therapy (SEACAT) evaluation, there is an evaluation of the phased introduction of combination anti-malarial therapy (CAT) in Mozambique, Swaziland and South Africa. In order to facilitate formulation of effective regional drug policy and provide a database for decision-making on the implementation of CAT, it is essential that the in vivo response to CAT be investigated. This will be achieved through the SEACAT 01 protocol which is a component of the SEACAT evaluation described in another file on this website. However, in selected Mozambique sites where the intensity of malaria transmission is high, a direct parallel group comparison of monotherapy (SP) with CAT (artesunate, AS, plus SP) will be conducted according to a specific amendment (Amendment 4) to the SEACAT 01 protocol. Amendment 4 is presented in this separate file on the website for clarity.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Sulfadoxine-pyrimethamine | Drug | |||
| Artesunate plus sulfadoxine-pyrimethamine | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| Therapeutic efficacy defined as: Adequate Clinical and Parasitological Response (ACPR), Early Treatment Failure (ETF), Late Treatment Failure (LTF), defined as Late Clinical Failure (LCF) and Late Parasitological Failure (LPF) | ||
| Sensitive or parasitological failure (RI, early and late, RII, RIII) | ||
| Parasitological failures will be classified as recrudescence or re-infection (or indeterminate) using GLURP and MSP I & II markers | ||
| Parasite clearance time | ||
| Fever clearance time |
| Measure | Description | Time Frame |
|---|---|---|
| Association between study treatment and gametocyte carriage | ||
| Pharmacokinetics by measurement of whole blood levels of Sulfadoxine and Pyrimethamine | ||
| Correlation of frequency of DHFR and DHPS mutations with parasitological outcome |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Karen Barnes, MBChB | University of Cape Town | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Catuane Clinic | Catuane | Matutuine | Mozambique | |||
| Namaacha Clinic |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 19558654 | Derived | Allen EN, Little F, Camba T, Cassam Y, Raman J, Boulle A, Barnes KI. Efficacy of sulphadoxine-pyrimethamine with or without artesunate for the treatment of uncomplicated Plasmodium falciparum malaria in southern Mozambique: a randomized controlled trial. Malar J. 2009 Jun 26;8:141. doi: 10.1186/1475-2875-8-141. |
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| ID | Term |
|---|---|
| D008288 | Malaria |
| ID | Term |
|---|---|
| D011528 | Protozoan Infections |
| D010272 | Parasitic Diseases |
| D007239 | Infections |
| D000096724 | Mosquito-Borne Diseases |
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| ID | Term |
|---|---|
| C001205 | fanasil, pyrimethamine drug combination |
| D000077332 | Artesunate |
| ID | Term |
|---|---|
| D037621 | Artemisinins |
| D017382 | Reactive Oxygen Species |
| D005609 | Free Radicals |
| D007287 | Inorganic Chemicals |
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| Tolerability by describing adverse events and changes in haematological parameters |
| Capacity by describing the training and development of study teams |
| Namaacha |
| Namaacha |
| Mozambique |
| D000079426 |
| Vector Borne Diseases |
| D009930 |
| Organic Chemicals |
| D012717 | Sesquiterpenes |
| D013729 | Terpenes |
| D006838 | Hydrocarbons |