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NCT Number: NCT01449045

Trial of Malaria Seasonal IPTc Combined With Community Case Management

Malaria is a major public health problem. 250 million cases annually leads to approximately 1 million deaths. Over 80 per cent of these deaths occur among African children under age five. The main interventions covered treatment with Artemisinin Combination Therapies (ACT), long lasting bednets distribution and Rapid Diagnosis Tests (RDT) to improve malaria diagnosis. This has led in Senegal to a substantial decrease in the incidence of malaria, in 2009. However the recent overall decline hides the fact that malaria incidence remains very high in the south of Senegal. That's why Home-based management (HMM) for malaria is being introduced in selected areas. Intermittent Preventive Treatment (IPT) by monthly administration of a therapeutic dose of antimalarials can achieve a very high degree of protection from attacks of clinical malaria in children. The purpose of this project is to evaluate the effectiveness of combining IPTc with HMM in southern Senegal

The study objectives are to :

* Assess the tolerance of IPTc using SP+AQ when it is administered for a longer period in areas with a longer transmission season, * Assess the added benefit that IPT with the association of Sulfadoxine-Pyrimethamine + Amodiaquine can offer in populations where a rapid and early care with home management of malaria is already established. * Determine the cost benefit ratio of the addition of IPTc with HMM. A cluster randomized controlled trial has been designed to evaluate the effectiveness of adding seasonal IPTc with sulfadoxine-pyrimethamine plus amodiaquine (SP+AQ) for 5 months per year, in villages where home-based management of malaria is implemented. All villages in Saraya district, excluding 7 villages with a health post, will be eligible to participate. Saraya villages will be combined to form 24 clusters which will be randomized to receive HMM from a community volunteer, or IPTc plus HMM. Trained volunteer Community Medicine Distributors (CMD) will provide HMM. The primary endpoint will be the incidence of clinical malaria with fever or history of fever and parasitaemia with density of at least 3000/ul. Secondary outcomes will include the safety, the tolerability, the coverage and acceptability of the intervention. Both the recurrent and capital costs to the health service of training staff and delivering the interventions will be estimated. Both direct and indirect costs to users of the services (children and their families) will also be assessed.

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Key information

Age range

3 month–10 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University Cheikh Anta Diop

Dakar, Senegal

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age between 3 to 120 months
  • consent participation given by parents or guardians
  • willing to remain in the study area in the next 6 months

Exclusion criteria

  • Known allergy to the study investigational drug
  • Any underlying chronic or severe condition.
  • Participant under Treatment with sulfamides

Treatment and study plan

IPTc+CCM

Drug

Monthly administration of sulfadoxine-pyrimethamine plus amodiaquine, combined with community case management

Community Case Management with artemether-lumefantrine (AL)

Drug

Malaria diagnosis with Rapid Diagnostic Test and treatment with AL if the test is positive

Primary outcomes

  1. Number of children under 10 years of age with clinical malaria

    Time frame: up to 24 weeks

    children under 10 years age presenting symptoms of malaria with fever (or history of fever in the previous 48 hours) with a positive Rapid Diagnostic Test or positive blood slides

Secondary outcomes

  1. Number of children under 10 years of age presenting clinical Malaria with high parasite density

    Time frame: up to 24 weeks

    Malaria with parasite density at 3000 parasites/uL or more in the presence of fever or history of fever in the previous 48hours in children under 10 years of age

Sponsors and collaborators

Lead sponsor

Cheikh Anta Diop University, Senegal

Other

Collaborators

  • London School of Hygiene and Tropical Medicine

Registry information

Official study title

Cluster Randomized Trial of Malaria Seasonal IPTc Combined With Community Case Management in Saraya District, SE Senegal

Important dates

Study start
2011
Primary completion
2011
Study completion
2012
First posted
Oct 7, 2011
Registry last updated
Apr 26, 2012

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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