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Seasonal Intermittent Preventive Treatment With Sulfadoxine-Pyrimethamine in Children in Mali

Evaluation of a Malaria Transmission Target Strategy Based on the Periodic Treatment With Sulfadoxine-Pyrimethamine vs. Early Case Management

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00623155
Enrollment
262
Registered
2008-02-25
Start date
2002-07-31
Completion date
2004-01-31
Last updated
2008-02-25

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

Conditions

Malaria

Keywords

malaria, intermittent preventive treatment, season, children

Brief summary

Recent, randomized controlled trials conducted in areas of perennial malaria transmission have shown that intermittent preventive treatment (IPT) given at the time of vaccination reduced the incidence of the first episode of malaria and severe anaemia during the first year of life by more than 50% without there being any rebound in the subsequent year. However, in countries such as Mali, where malaria is highly seasonal and prevalent in older children, IPT in infants may not be the optimum way in which to use antimalarial drugs to prevent malaria. An alternative approach is to give intermittent preventive treatment to children at risk just during the rainy season. Here we propose (i) to evaluate the impact of two seasonal IPT (sIPT) with Sulfadoxine-pyrimethamine (SP) given at 8 weeks interval on the incidence of malaria disease in children of 6 months to 10 years in an area of seasonal transmission, in Kambila, Mali; (ii) to assess the impact of this strategy on the in vivo response of P. falciparum to SP; (iii) to assess the potential rebound effect of this strategy on the subsequent transmission season after the cessation. Children 6 months-10 years in Kambila, Mali will randomized to receive either IPT with SP twice at 8 weeks interval or no IPT during the transmission season and will followed up for 12 months. Subjects will be also followed during the subsequent transmission season to assess possible rebound effect. Clinical malaria cases will be treated with SP and followed for 28 days to assess the in vivo response during both periods.

Interventions

DRUGSeasonal IPT in children - Sulfadoxine-pyrimethamine

Subjecs randomized to receive two intermittent preventive treatments with standard recommended treatment doses of Sulfadoxine-pyrimethamine at 8 weeks interval during the peak malaria transmission season.

Sponsors

World Health Organization
CollaboratorOTHER
University of Bamako
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Months to 10 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 6 months to 10 years * Agree to seek initial medical care for all medical illness in the study clinic during the study period * Written informed consent by a parent or legal garden, * No plan to travel for a long time during the study period.

Exclusion criteria

* History of allergy to sulfa drugs or Sulfadoxine-pyrimethamine * Chronic illness or symptomatic malaria at the time of enrollment

Design outcomes

Primary

MeasureTime frame
incidence rate of clinical malaria
in vivo adequate clinical and parasitological response of P. falciparum to SP

Countries

Mali

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 5, 2026