Spatial Repellents for Malaria Control
NCT06122142 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2025-03-07
Summary
The primary objective of the study is to demonstrate and quantify the effectiveness of a spatial repellent (SR) product, in reducing malaria infection in humans under operational program conditions in a humanitarian assistance context. The design will be a cluster Randomized Control Trial (cRCT) representing an operational research study.
Conditions
Interventions
- DEVICE
-
Transfluthrin - delivery by paid study personnel
Passive emanator with formulated transfluthrin, SR product will be delivered by paid study personnel
- DEVICE
-
Transfluthrin - delivery by voucher system
Passive emanator with formulated transfluthrin, voucher which will be used to redeem for SR product(s) on a monthly basis for each head of household.
- DEVICE
-
Transfluthrin - delivery by village health teams
Passive emanator with formulated transfluthrin, village health teams will distribute SR products.
Sponsors & Collaborators
-
S.C. Johnson & Son, Inc.
collaborator INDUSTRY -
Catholic Relief Services
collaborator OTHER -
Infectious Diseases Research Collaboration, Uganda
collaborator OTHER -
University of Notre Dame
lead OTHER
Principal Investigators
-
John P Grieco, Ph.D. · University of Notre Dame
-
Suzanne Van Hulle, M.H.S. · Catholic Relief Services
Study Design
- Allocation
- RANDOMIZED
- Purpose
- PREVENTION
- Masking
- QUADRUPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 6 Months
- Max Age
- 59 Months
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-05-31
- Primary Completion
- 2025-05-31
- Completion
- 2025-05-31
Countries
- Uganda
Study Locations
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