Normal Immunological Parameters Among Healthy Volunteers in Kambila, Mali
NCT ID: NCT00471302
Last Updated: 2022-06-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
310 participants
OBSERVATIONAL
2007-08-01
2022-05-23
Brief Summary
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People 18 years of age or older who live in Kambila, Tieneguebougou or Kalifabougou, Mali, and are in good health may be eligible for this study.
Participants undergo a complete physical examination at the start of the study and then once a year for the 4-year duration of the study. They have a maximum of nine clinic visits a year to collect blood samples for research. The visits last about one hour, including a 30-minute observation time after the blood draw.
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Detailed Description
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against Plasmodium falciparum is regarded as a crucial step toward control of this disease. Unfortunately, vaccine
candidates have resulted in short-lived protection at best. The ineffectiveness of current vaccines may reflect the kinetics
of naturally acquired immunity to malaria in that multiple infections are required over years before partial protection is
achieved and then immunity is lost, or becomes less effective, in the absence of recurrent infection. The mechanisms
underlying the delayed acquisition and presumably rapid loss of humoral immunity are poorly understood. A more
detailed understanding of these processes at the cellular level may be important for vaccine development. We are
currently studying the cellular basis of humoral immunity to P. falciparum through research collaboration between the
Malaria Research and Training Center (MRTC) in Bamako, Mali and the National Institutes of Health (NIH) in the United
States. This protocol supports that research by ensuring a supply of blood samples from healthy Malian adults in order to
establish normal immunologic parameters for this population and to optimize research assays performed at the MRTC.
Conditions
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Study Design
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CASE_ONLY
CROSS_SECTIONAL
Study Groups
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1
Healthy adults in a malaria endemic area in Mali
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Resident of Kambila, Tieneguebougou or Kalifabougou
* Adequate venous access
* Willingness to allow blood samples to be stored and used for future studies of the immune response to malaria
* Ability to give informed consent and willingness to comply with study requirements and procedures
Exclusion Criteria
* Currently taking antimalarials, corticosteroids or other immunosuppressants.
* Underlying heart disease, bleeding disorder, or other conditions that in the judgment of the Principal Investigator (PI) could increase the risk to the volunteer.
* Fever greater than or equal to 37.5 degrees Celsius or evidence of an acute infection.
* Current pregnancy, as determined by urine dipstick test for pregnancy.
* Participation in another clinical protocol that requires the administration of an experimental vaccine or experimental treatment.
18 Years
55 Years
ALL
Yes
Sponsors
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University of Bamako
OTHER
National Institute of Allergy and Infectious Diseases (NIAID)
NIH
Responsible Party
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Principal Investigators
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Peter D Crompton, M.D.
Role: PRINCIPAL_INVESTIGATOR
National Institute of Allergy and Infectious Diseases (NIAID)
Locations
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U Mali Faculty Med Pharmacy & Dentistry IRB #1
Bamako, , Mali
Countries
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Other Identifiers
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07-I-N141
Identifier Type: -
Identifier Source: secondary_id
999907141
Identifier Type: -
Identifier Source: org_study_id
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