Spatial Repellents for Vector Control (AEGIS Mali)
Primary Purpose
Malaria
Status
Active
Phase
Not Applicable
Locations
Mali
Study Type
Interventional
Intervention
Transfluthrin
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Malaria focused on measuring Malaria, Spatial Repellent, Transfluthrin, Vector-borne diseases, Mosquito vectors, Incidence
Eligibility Criteria
Inclusion Criteria:
- Children ≥ 6 months to < 10 years of age
- Children with Hb > 7 g/dL and no signs of known chronic disease or other other serious illness
- Sleeps in cluster ≥ 90% of nights during any given month
- Not participating in another clinical trial investigating a vaccine, drug, medical device, or a medical procedure during the trial
- Provision of informed consent (and/or assent) form (ICF) signed by the parent(s) or guardian
Exclusion Criteria:
- Children < 6 months or ≥ 10 years
- Childrend with Hb <= 7 g/dL with signs of known chronic disease or other serious illness, or Hb <6 g/dL with signs of clinical decompensation
- Sleeps in cluster <90% of nights during any given month
- Participating or planned participation in another clinical trial investigating a vaccine, drug, medical device, or a medical procedure during the trial
- No provision of ICF (and/or assent) signed by the parent(s) or guardian
Sites / Locations
- Catholic Relief Services
- Malaria Research and Training Center (MRTC), University of Bamako, Mali
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Spatial Repellent
Placebo
Arm Description
Transfluthrin
Inert ingredients
Outcomes
Primary Outcome Measures
Number of first-time malaria infections during intervention period.
Measured by microscopy in children aged between 6 months to 10 years.
Secondary Outcome Measures
Number of overall new malaria infections during intervention period.
Measured by microscopy in children aged between 6 months to 10 years.
Parasite-species-specific first-time malaria infections.
Measured by microscopy in children aged between 6 months to 10 years.
Parasite-species-specific overall malaria infections.
Measured by microscopy in children aged between 6 months to 10 years.
Number of first-time malaria infections by two age groups (≤ 59 months old; 5 years old to 10 years old).
Measured by microscopy in children aged between 6 months to 10 years.
Number of overall malaria infections by two age groups (≤ 59 months old; 5 years to 10 years old).
Measured by microscopy in children aged between 6 months to 10 years.
Anopheline-human contact (indoor and outdoor) using human biting rate (HBR) as an indicator for all anophelines and by anopheline species.
Measured by human-landing catch (HLC) during 12-h intervals on a quarterly basis during intervention period.
Anopheline parity rate as an indicator of population age structure for all anophelines and by anopheline species.
Measured by mosquito ovarian dissections from a sub-sample of anophelines collected during HLC procedures during intervention period.
Anopheline infectivity using sporozoite rate as an indicator for all anophelines and by anopheline species.
Measured by laboratory detection of sporozoites in mosquito head-preps from a sub-sample of anophelines collected during HLC and/or CDC-light trap procedures during intervention period.
Anopheline infectivity using entomological inoculation rate (EIR) as an indicator for all anophelines and by anopheline species.
Measured by calculating the number of sporozoite-infected anopheline mosquitoes captured per person during intervention period from HLC and/or CDC-light trap procedures.
CDC-light trap indoor density for all anophelines and by anopheline species.
Measured by CDC-light trap collections during 12-h intervals on a monthly basis during intervention period.
Insecticide resistance.
Measured by WHO filter paper test and CDC bottle assays during baseline and intervention period.
Adverse Events and Serious Adverse Events.
Measured by solicited and unsolicited reports during baseline and intervention period. Mean, minimum and maximum frequency and percentage of Adverse Events(AEs) and Severe Adverse Events (SAEs) across clusters among enrolled subjects will be summarized by treatment arm.
Full Information
NCT ID
NCT04795648
First Posted
March 9, 2021
Last Updated
April 29, 2022
Sponsor
University of Notre Dame
Collaborators
SC Johnson, A Family Company, fhiClinical, Malaria Research and Training Center, Bamako, Mali, Catholic Relief Services
1. Study Identification
Unique Protocol Identification Number
NCT04795648
Brief Title
Spatial Repellents for Vector Control
Acronym
AEGIS Mali
Official Title
Spatial Repellent Products for Control of Vector Borne Diseases
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 8, 2021 (Actual)
Primary Completion Date
October 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Notre Dame
Collaborators
SC Johnson, A Family Company, fhiClinical, Malaria Research and Training Center, Bamako, Mali, Catholic Relief Services
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The primary objective of the study is to demonstrate and quantify the protective efficacy of a single Spatial Repellent (SR) product, in reducing malaria infection in a human cohort. The study design will be a prospective cluster Randomized Control Trial (cRCT).
Detailed Description
Children ≥ 6 months to < 10 years of age will be enrolled in a single cohort across 60 clusters (30 clusters per treatment arm). The cohort will be followed for 6 months for baseline covariate measurements and 24 months with intervention. Blood samples will be taken once every 4 weeks from all cohort subjects to test for malaria infection and whenever a subject reports a recent history of fever (within previous 48 hours). During follow up of enrolled subjects, study clinicians will have the option to conduct a Hb test for enrolled subjects when they may present signs of anemia to see if they might need additional treatment beyond malaria ACTs (if malaria infection is indicated). Rapid Diagnostic Tests (RDTs) will be used for point-of-care diagnosis of malaria infection with microscopy used to confirm infection status. All positive malaria infections as indicated by either RDT or microscopy, clinical and asymptomatic, will be treated. If a subject has a RDT negative outcome but a positive microscopy diagnosis, follow up treatment for the malaria infection will be provided to the subject within 72hrs of the microscopy read. Cohort subjects who test positive for malaria by either RDT or microscopy, symptomatic or asymptomatic, during both scheduled and unscheduled visits will be treated with ACTs. The incidence of malaria infection will be measured by microscopy and estimated and compared between treatment arms to determine the benefit of using an SR in an area with high, seasonal transmission of malaria.
Entomological endpoints of exposure risk to mosquitoes will also be measured to identify entomological correlates of SR efficacy that may be useful for the evaluation of new SR products. Twenty clusters (10 SR, 10 placebo) will be randomly selected to estimate the impact of the SR on entomological measures of malaria transmission. Within each cluster, light trap collections will be conducted monthly in 10 randomly selected households to assess the impact of SRs on the density of Anopheles mosquitoes indoors. Human landing catches will be done indoors and outdoors in 6 intervention and 6 control clusters (the 12 clusters will remain fixed throughout the study) in four houses (randomly selected) in each cluster for the period of 2 nights (total of 48 houses across both arms) once every quarter (3 months) to determine the effect of SR on the host seeking behavior of mosquitoes.
The SR will be a new formulation of transfluthrin. This active ingredient (AI) is widely used in mosquito coils and other household pest control products. The new formulation is a passive emanator that will release the AI over a period of up to four weeks. The emanator will consist of a pre-treated piece of cellulose acetate, which will be positioned within consenting households according to manufacturer specifications. The SRs and placebos for this study will be designed and manufactured by S.C. Johnson, Inc. USA.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria
Keywords
Malaria, Spatial Repellent, Transfluthrin, Vector-borne diseases, Mosquito vectors, Incidence
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study design will be a prospective cluster Randomized Control Trial (cRCT)
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
1920 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Spatial Repellent
Arm Type
Experimental
Arm Description
Transfluthrin
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Inert ingredients
Intervention Type
Device
Intervention Name(s)
Transfluthrin
Intervention Description
Passive emanator with formulated transfluthrin
Intervention Type
Device
Intervention Name(s)
Placebo
Intervention Description
Passive emanator with formulated inert ingredients
Primary Outcome Measure Information:
Title
Number of first-time malaria infections during intervention period.
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Number of overall new malaria infections during intervention period.
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Title
Parasite-species-specific first-time malaria infections.
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Title
Parasite-species-specific overall malaria infections.
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Title
Number of first-time malaria infections by two age groups (≤ 59 months old; 5 years old to 10 years old).
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Title
Number of overall malaria infections by two age groups (≤ 59 months old; 5 years to 10 years old).
Description
Measured by microscopy in children aged between 6 months to 10 years.
Time Frame
24 months
Title
Anopheline-human contact (indoor and outdoor) using human biting rate (HBR) as an indicator for all anophelines and by anopheline species.
Description
Measured by human-landing catch (HLC) during 12-h intervals on a quarterly basis during intervention period.
Time Frame
24 months
Title
Anopheline parity rate as an indicator of population age structure for all anophelines and by anopheline species.
Description
Measured by mosquito ovarian dissections from a sub-sample of anophelines collected during HLC procedures during intervention period.
Time Frame
24 months
Title
Anopheline infectivity using sporozoite rate as an indicator for all anophelines and by anopheline species.
Description
Measured by laboratory detection of sporozoites in mosquito head-preps from a sub-sample of anophelines collected during HLC and/or CDC-light trap procedures during intervention period.
Time Frame
24 months
Title
Anopheline infectivity using entomological inoculation rate (EIR) as an indicator for all anophelines and by anopheline species.
Description
Measured by calculating the number of sporozoite-infected anopheline mosquitoes captured per person during intervention period from HLC and/or CDC-light trap procedures.
Time Frame
24 months
Title
CDC-light trap indoor density for all anophelines and by anopheline species.
Description
Measured by CDC-light trap collections during 12-h intervals on a monthly basis during intervention period.
Time Frame
24 months
Title
Insecticide resistance.
Description
Measured by WHO filter paper test and CDC bottle assays during baseline and intervention period.
Time Frame
30 months
Title
Adverse Events and Serious Adverse Events.
Description
Measured by solicited and unsolicited reports during baseline and intervention period. Mean, minimum and maximum frequency and percentage of Adverse Events(AEs) and Severe Adverse Events (SAEs) across clusters among enrolled subjects will be summarized by treatment arm.
Time Frame
30 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
10 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Children ≥ 6 months to < 10 years of age
Children with Hb > 7 g/dL and no signs of known chronic disease or other other serious illness
Sleeps in cluster ≥ 90% of nights during any given month
Not participating in another clinical trial investigating a vaccine, drug, medical device, or a medical procedure during the trial
Provision of informed consent (and/or assent) form (ICF) signed by the parent(s) or guardian
Exclusion Criteria:
Children < 6 months or ≥ 10 years
Childrend with Hb <= 7 g/dL with signs of known chronic disease or other serious illness, or Hb <6 g/dL with signs of clinical decompensation
Sleeps in cluster <90% of nights during any given month
Participating or planned participation in another clinical trial investigating a vaccine, drug, medical device, or a medical procedure during the trial
No provision of ICF (and/or assent) signed by the parent(s) or guardian
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John P Grieco, Ph.D.
Organizational Affiliation
University of Notre Dame
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Suzanne Van Hulle, M.H.S
Organizational Affiliation
Catholic Relief Services
Official's Role
Principal Investigator
Facility Information:
Facility Name
Catholic Relief Services
City
Bamako
Country
Mali
Facility Name
Malaria Research and Training Center (MRTC), University of Bamako, Mali
City
Bamako
Country
Mali
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Analytical datasets will be anonymized and GPS tag-blurred to remove sensitive information prior to sharing.
IPD Sharing Time Frame
The data and supporting information will be made available 12 months following completion of data analysis and will remain open access in the public domain.
IPD Sharing Access Criteria
Open-access repository distributed under the terms of the Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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Links:
URL
http://www.sante.gov.ml/index.php/annuaires/download/4-systeme-local-d-information-sanitaire-slis/6-annuaire-statistique-2018-du-systeme-local-d-information-sanitaire-du-mali
Description
Annuaire Statistique 2018 du Systeme Local d'Information Sanitaire (SLIS) du Mali, 2018
URL
https://dhsprogram.com/pubs/pdf/SR261/SR261.E.pdf
Description
Demographic Health Survey, Mali, 2018
URL
https://dhsprogram.com/what-we-do/survey/survey-display-487.cfm
Description
Demographic Health Survey, Mali, 2015
URL
https://www.dhis2.org/about
Description
Health Management Information System, DHIS2, 2018
URL
https://catalog.ihsn.org/index.php/catalog/4569
Description
Recensement General de la Population et de l'Habitat du Mali (RGPH) 2009
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Spatial Repellents for Vector Control
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