National Public Health Institute of Liberia (NPHIL)
Fleh-la, Liberia
NCT Number: NCT04704674
Background:
Malaria is a disease that affects many people in Liberia. It is caused by germs (parasites) that are spread by mosquito bites. Researchers want to gather data that may help them understand the best way to use a malaria vaccine in Liberia, which will be important in getting rid of the disease.
Objective:
To find out how often people of all ages who live in Fleh-la and Marshansue, Liberia, get malaria.
Eligibility:
Healthy people ages 6 months and older who live in Fleh-la and Marshansue in a household with adults and children.
Design:
Participants will be screened with a physical exam and questions about their health.
Participants will have monthly study visits. They will be asked about any symptoms of malaria and their use of bednets. Their vital signs, such as blood pressure and temperature, will be checked. Blood will be taken from the participant s arm or finger with a needle. If they have a fever, they will get a malaria test. If positive, they will get drugs to treat malaria.
Once a month, participants houses will be examined for mosquitoes. The team will remove all mosquitoes they collect. As part of this collection, participants houses will be sprayed with a chemical to kill mosquitoes and other insects. Participants will not be allowed in their house while the team is inside. The spray will not harm the participants.
Once a year, at the monthly visit, an additional blood sample will be taken.
Some of the participants blood samples will be used for genetic testing.
Participation will last for up to 3 years.
This study is active but is not currently recruiting participants.
Notify Me6 month and older
All sexes
Observational
Fleh-la, Liberia
A vaccine that interrupts malaria transmission is critical to eradicate the disease, but improved assays are needed to measure the efficacy of vaccines. Transmission-blocking vaccines (TBVs) work by inducing antibodies that inhibit parasite development in the mosquito interrupting transmission. Efficacy of vaccines may be estimated by in vitro membrane feeding assays using immune sera and laboratory mosquitoes, but qualified assays that measure transmission in the field are needed to assess transmission-blocking interventions in natura. Clinical trials of TBVs have started elsewhere on the continent in Mali, and we have planned to expand TBV studies here in Liberia soon. This protocol is already being used for a longitudinal cohort to gather information of malaria transmission based on the rates of blood smear positive individuals by month, season and year in Fleh-la and Marshansue, in Salala, Bong County, Liberia. Individuals in the villages were approached first for participation, including permission to contact their household and neighbors of their compound for participation. Households were identified using census data and individuals who consented for participation are being enrolled. Malaria smears are obtained at monthly visits, in conjunction with mosquito collections in/around village residences. Parasite infection rates in locally caught mosquitoes will be assessed longitudinally for differences by season and year. A total of 400 volunteers from Fleh-la and Marshansue will be enrolled. Participants will be followed for at least one year, to collect data that will guide the design of future community-based trials of TBV for which this amendment is being submitted for approval.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Subject Inclusion Criteria:
Household Inclusion Criteria:
To be eligible for participation, households must meet the following criteria:
Exclusion criteria
Subject Exclusion Criteria:
Time frame: one year
Rate of blood smear positive individuals
National Institute of Allergy and Infectious Diseases (NIAID)
Nih
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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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