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A trial of targetted control to eliminate malaria in Central Senegal

Randomized trial of spatially targetted malaria control to virtually eliminate malaria in areas of very low incidence and patchy transmission in Senegal.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR201310000575267
Enrollment
497379
Registered
2013-06-27
Start date
2013-06-16
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Malaria

Interventions

Mass Screening And Treatment
Insecticide residual spraying
MSAT
IRS+MDA
Control

Sponsors

Universite Cheikh Anta Diop, Dakar
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: In each year of intervention, hotspot areas will be defined on the basis of the previous year¿s malaria cases. Within the hotspots in the intervention clusters, all households will be offered IRS spraying, and all persons over 3 months of age will be included in MDA and MSAT rounds. For the cross sectional survey each year, participants (all ages, both genders) will be selected randomly from the DSS database, all selected persons who consent to participate will be included. Pregnant women will be eligible for treatment with DHA-PQ if they are in the second or third trimester (more than 3 months since last menstrual period, or after quickening (first movements of the baby detected by the mother).

Exclusion criteria

Exclusion criteria: Health posts in urban and semi-urban areas will be excluded. Households will be excluded from IRS if the head of the household does not consent. They will remain eligible for other aspects of the trial. In MDA and MSAT arms, households will not be included if the head of the household refuses. Individuals will be included only if they (or their mother/carer) consent. In the MDA arm of the trial, treatment with DHA-PQ will be withheld from babies under 3 months of age, from person with history of allergy to ACTs, from persons who are unwell and require medical attention, and from women who say they are pregnant. Persons who are unwell will be referred to the nearest health facility. In the MSAT arm, babies under 3 months of age will not be screened. Women in the first trimester of pregnancy (pregnant for less than 3 months) and women who believe they may be pregnant, who test positive for malaria by RDT, and persons with known allergy to ACTs who test positive by RDT, will not be treated with DHA-PQ, they will be given a referral card with their test result and referred for treatment at the nearest health post. Persons who are unwell with fever will be tested and treated with DHA-PQ if positive, or referred, in accordance with national guidelines for community case

Design outcomes

Primary

MeasureTime frame
Prevalence of malaria infection and incidence of malaria in year 2

Secondary

MeasureTime frame
Prevalence of malaria infection in the hotspots;Incidence of malaria and prevalence of malaria infection in targetted and non-targetted areas in year 1 and year 2;Incidence of severe adverse events within 10 days of drug administration;Coverage of and adherence to the interventions;The prevalence of molecular markers associated with resistance to PQ;Costs of the interventions;Prevalence of infection by PCR and prevalence by serology

Countries

Senegal

Contacts

Public ContactPaul;Oumar Milligan;Gaye

Reader LSHTM;Professor UCAD

paul.milligan@lshtm.ac.uk;ogaye@refer.sn+44 (0)20 7636 8636;+221-33 825 19 99

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026