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Adjunctive Ivermectin Mass Drug Administration for Malaria Control

Adjunctive Ivermectin Mass Drug Administration for Malaria Control on the Bijagos Archipelago of Guinea Bissau: A Cluster-randomized Placebo-controlled Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04844905
Acronym
MATAMAL
Enrollment
24000
Registered
2021-04-14
Start date
2021-05-03
Completion date
2023-08-31
Last updated
2022-02-24

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

Conditions

Hook Worm, Lymphatic Filariasis, Malaria,Falciparum, Neglected Tropical Diseases, Scabies, Soil Transmitted Helminths, Strongyloidiasis

Keywords

Vector Control, Mass Drug Administration, Integrated Disease Control, Malaria, Guinea Bissau, West Africa, Antimalarials, Ivermectin, Dihydroartemisinin, Piperaquine

Brief summary

This is a cluster-randomized placebo-controlled clinical trial to evaluate the additive benefit of Ivermectin (IVM) (or Placebo) mass drug administration (MDA) to dihydroartemisinin-piperaquine (DP) MDA for malaria control in a moderate to low malaria-endemic setting as an adjunctive strategy to existing programmatic malaria control measures. The regime of DP and IVM will target both human reservoirs of Plasmodium falciparum and the Anopheles gambiae vector respectively, with the aim of interrupting transmission. The trial will be conducted on the Bijagos Archipelago, where islands (clusters) will be randomised to receive seasonal DP and IVM or DP and Placebo MDA. The primary outcome will be the prevalence of infection with Plasmodium falciparum in all age groups detected by nucleic acid amplification testing during the peak malaria transmission season after two years of intervention.

Detailed description

The objectives of this trial are 1. To evaluate the impact of adjunctive IVM to DP MDA on malaria transmission in communities with high ITN coverage. 2. To evaluate the impact of IVM MDA on An. gambiae population density and age-structure. 3. To evaluate the impact of IVM MDA on the prevalence of co-endemic IVM-susceptible Neglected Tropical Diseases (lymphatic filariasis, soil transmitted helminths and scabies) 4. To evaluate acceptability, feasibility and access to MDA as a strategy for malaria control and to identify the most acceptable way of achieving and sustaining high coverage MDA with IVM and DP. This cluster-randomized placebo-controlled trial has two arms. A total of 24 clusters will be randomly assigned to receive DP + IVM MDA or DP+ Placebo MDA using computer-generated random numbers. To mitigate against contamination effects, the majority of clusters will be separate islands and will be separated by distances greater than 2km. On the two islands that are divided (each into two clusters), a buffer zone of 2km between each cluster will be ensured. The total population of the archipelago is 24,000. The investigators will ensure balance between trial arms with respect to population size, baseline Plasmodium falciparum prevalence and access to health care. All clusters will receive the standard programmatic malaria control interventions implemented by the National Malaria Control Programme which includes insecticide-treated nets (ITN), intermittent preventative treatment in pregnancy (IPTp), seasonal malarial chemoprophylaxis (SMC) for children aged 3-59 months and case diagnosis and treatment (CDT) with Artemether-lumefantrine.

Interventions

DRUGIvermectin

Ivermectin will be given as tablets of 3 or 6mg. It will be given at 300-400μg/kg/day for 3 days (to the nearest whole tablet) each month for 3 months. It will be taken on an empty stomach with water.

DRUGPlacebo

Placebo will be given as tablets of 3 or 6mg (identical to Ivermectin in colour, size, shape and packaging). It will be given at 300-400μg/kg/day for 3 days (to the nearest whole tablet) each month for 3 months. It will be taken by mouth with water and without food.

DRUGDihydroartemisinin-piperaquine

Dihydroartemisinin-piperaquine will be given as tablets of 320/40mg (adult) and 160/20mg (child) piperaquine/dihydroartemisinin per tablet. Administration of a full course of dihydroartemisinin-piperaquine will be given in accordance with the manufacturer's guidelines once daily for 3 days each month for 3 months according to body weight. Dihydroartemisinin-piperaquine will be taken by mouth with water and without food.

Sponsors

Medical Research Council Unit, The Gambia
CollaboratorOTHER
Ministerio de Saude Publica, Guinee-Bissau
CollaboratorUNKNOWN
Bandim Health Project
CollaboratorOTHER
Instituto Nacional de Estudos e Pesquisas, Guinee-Bissau
CollaboratorUNKNOWN
London School of Hygiene and Tropical Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

An independent statistician will randomize the clusters to DP+IVM or DP+Placebo. The Placebo is identical in size, shape and colour and packaging. An independent pharmacist at Medical Research Council Unit The Gambia @ London School of Hygiene and Tropical Medicine will label the IVM and Placebo according to the statistician's designation and maintain the masking from all other investigators. Specifically generated masking codes will be generated and saved in three separate encrypted locations securely. Only the statistician and the pharmacist will have access to the encryption key.

Intervention model description

Two arms with clusters randomized to DP+IVM or DP+Placebo with a 1:1 ratio

Eligibility

Sex/Gender
ALL
Age
6 Months to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Age over six months to receive dihydroartemisinin-piperaquine 2. Height over 90cm or weight over 15kg to receive ivermectin or placebo 3. Willingness to adhere to trial procedures 4. Individual written, informed consent from the participant or parent/guardian in the case of participants below the age of 18 years (and assent in young people between the ages of 12 and 17 years of age)

Exclusion criteria

1. Known severe chronic illness (AIDS, Tuberculosis, chronic malnutrition) 2. Known hypersensitivity to either dihydroartemisinin-piperaquine or ivermectin 3. Pregnancy (any trimester) and breastfeeding (for ivermectin (or placebo)) and pregnancy (first trimester only) (for dihydroartemisinin-piperaquine) 4. Travel to a Loa loa endemic country (eg Central African Republic) (for ivermectin (or placebo)) 5. Concomitant drugs that influence cardiac function or affect the corrected QT interval (for dihydroartemisinin-piperaquine)

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of infection with Plasmodium falciparum2 yearsPrevalence of infection with Plasmodium falciparum in all age groups estimated using a cross-sectional survey sample conducted during peak transmission season after 2 years of intervention

Secondary

MeasureTime frameDescription
Prevalence of infection with Plasmodium falciparum1 yearPrevalence of infection with Plasmodium falciparum in all age groups estimated using a cross-sectional survey sample conducted after the first year of intervention
Incidence of clinical malaria (Passive Case Detection)For six months during the malaria transmission seasonIncidence of clinical malaria diagnosed at health facilities confirmed by malaria Rapid Diagnostic Test
Incidence of clinical malaria (Active Case Detection)For six months during the malaria transmission seasonIncidence of clinical malaria confirmed by malaria Rapid Diagnostic Test in a cohort of 50 children per cluster aged 5-14 years
Age-adjusted prevalence of recent exposure to Plasmodium falciparumPeak transmission season at 1 year and 2 yearsMean Median Fluorescence Intensity of serological markers associated with recent exposure to Plasmodium falciparum in all age groups estimated using a cross-sectional survey sample during peak transmission season after each year of intervention
Vector densityFor six months during the malaria transmission seasonTotal number of trapped mosquitoes per cluster
Vector parous rate7-14 days post-MDAVector parous rate will be determined by assessment of mosquitoes trapped 7-14 days following MDA. Vector parity will be used to determine Anopheles gambiae age structure to estimate vector survival between arms.
Prevalence of exposure to Anopheles exposurePeak transmission season at 1 year and 2 yearsMean Median Fluorescence Intensity of serological markers associated with exposure to Anopheles salivary antigen in all age groups estimated using a cross-sectional survey sample
Vector sporozoite ratesFor six months during the malaria transmission seasonProportion of Plasmodium falciparum circumsporozoite antibody (CSP) positive mosquitoes caught in traps
Prevalence of Ivermectin-susceptible Neglected Tropical Diseases (NTDs)2 yearsPrevalence of IVM-susceptible NTDs (scabies, strongyloides, other soil-transmitted helminths and lymphatic filariasis) and head lice using clinical and serological parameters estimated using a cross-sectional survey sample during the dry season after two years of intervention.
MDA coverage estimatesDuring MDA in year 1 and year 2Cluster level coverage estimates calculated from MDA distribution and denominator census
Prevalence of resistance to artemisinin and partner drugs in humansPeak transmission season at 1 year and at 2 yearsPrevalence of resistance to artemisinin and partner drugs in humans using molecular markers of resistance in all age groups estimated using a cross-sectional survey sample
Vector species compositionFor six months during the malaria transmission seasonSpecies characterisation using nucleic acid amplification tests as a proportion of total mosquitoes caught in traps

Countries

Guinea-Bissau

Contacts

Primary ContactAnna R Last, MBChB PhD
anna.last@lshtm.ac.uk0044(0)2072770
Backup ContactDavid CW Mabey
david.mabey@lshtm.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026