NCT Number: NCT00203736
A Randomised Efficacy Study of Combination Antimalarials to Treat Uncomplicated Malaria
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.
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Notify MeKey information
Conditions
Age range
12 month and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Catuane Clinic, Catuane, Matutuine, Mozambique
About this study
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.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Male or female, older than 12 months.
- Weight > 10 kg.
- Diagnoses of uncomplicated acute P. falciparum malaria parasitaemia of up to 500 000 asexual parasite/mcl blood with axillary temperature of greater than and equal to 37.50C or history of fever.
- Documented informed consent.
- Lives close enough to the health centre for reliable follow up.
Exclusion criteria
- Has received anti-malarial treatment in the past 7 days.
- Is infected with other malarial species (such subjects will be excluded retrospectively).
- Severely ill (based on WHO Criteria for severe malaria ) or if patient is considered, in the opinion of the investigator or designee, to have moderately severe malaria (e.g. prostrate, repeated vomiting, dehydrated).
- Has received cotrimoxazole or chloramphenicol in the past 7 days.
- History of G6PD deficiency.
- Is pregnant.
- Has a history of allergy to any sulphonamide (for SP) or artemisinin derivative (for artesunate and co-artemether).
Treatment and study plan
Artesunate plus sulfadoxine-pyrimethamine
DrugPrimary outcomes
-
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)
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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
Secondary outcomes
-
Association between study treatment and gametocyte carriage
-
Pharmacokinetics by measurement of whole blood levels of Sulfadoxine and Pyrimethamine
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Correlation of frequency of DHFR and DHPS mutations with parasitological outcome
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Tolerability by describing adverse events and changes in haematological parameters
-
Capacity by describing the training and development of study teams
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Lead sponsor
University of Cape Town
Other
Collaborators
- Global Fund
- Medical Research Council, South Africa
- World Health Organization
Registry information
Official study title
Open Label Drug Study (With Single and Parallel Group Components) to Evaluate Combination Antimalarial Therapy for Efficacy, Gametocyte Carriage and Molecular Markers Associated With SP Resistance in Uncomplicated Plasmodium Falciparum Infections
Important dates
- Study start
- 2003
- Study completion
- 2003
- First posted
- Sep 20, 2005
- Registry last updated
- Nov 16, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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