Malaria Clinical Trial
Official title:
Coinfection With Plasmodium Falciparum and Wuchereria Bancrofti: Clinical, Epidemiologic and Immunologic Implications
Verified date | January 31, 2012 |
Source | National Institutes of Health Clinical Center (CC) |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study will examine the clinical, immunological and epidemiological effects of concurrent
infections with P. falciparum and W. bancrofti or M. perstans (the parasites that cause
malaria and filariasis) on the frequency and severity of malaria infection in children and
young adults in Mali, Africa.
Residents of Tien gu bougou and Bougoudiana, Mali, who are between 1 and 20 years of age may
be eligible for this study. Participants with and without filarial infection will be
enrolled.
Participants undergo the following tests and procedures:
- Baseline evaluation with medical history and physical examination, blood tests and stool
culture
- Brief physical examinations weekly
- Blood tests monthly for malaria
- Standard treatment offered for anyone with malaria
- Blood tests for filarial infection at the beginning, midpoint and end of the
transmission season
- Treatment for lymphatic filariasis is available through the National Program for the
Elimination of Lymphatic Filariasis. There is no effective standard therapy for M.
perstans.
- Treatment for other parasitic worm infections, if needed.
Status | Completed |
Enrollment | 1039 |
Est. completion date | January 31, 2012 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | All |
Age group | 1 Year to 20 Years |
Eligibility |
- INCLUSION CRITERIA (Screening): Age 1 - 20 years Male or non-pregnant female Resident of Tien gu bougou or Bougoudiana EXCLUSION CRITERIA (Screening): History or clinical evidence of severe and/or chronic illness History of allergy to artesunate, amodiaquine, albendazole, praziquantel or mebendazole Plans to relocate outside the immediate vicinity of the village during the study period INCLUSION CRITERIA (Matched prospective study): Age 1 - 20 years Male or non-pregnant female Resident of Tien gu bougou or Bougoudiana EXCLUSION CRITERIA (Matched prospective study): History or clinical evidence of severe and/or chronic illness History of allergy to artesunate, amodiaquine, albendazole, praziquantel or mebendazole Plans to relocate outside the immediate vicinity of the village during the study period Hemoglobin less than or equal to 8 g/dL Symptoms of malaria with parasitemia greater than or equal to 100,000/microliters at enrollment Recent history or clinical evidence of prostration, bleeding, respiratory distress, seizures, coma or obtundation, jaundice, inability to drink, persistent vomiting INCLUSION CRITERIA: (Immunologic Extension Study) Age > 10 years Male or non-pregnant female (by history) Resident of Tien gu bougou or Bougoudiana Willingness to allow storage of specimens for future research EXCLUSION CRITERIA: (Immunologic Extension Study) History or clinical evidence of severe and/or chronic illness Hemoglobin less than or equal to g/dL Positive pregnancy test Clinical malaria (symptoms of malaria plus any malaria parasites identified on thick smear) |
Country | Name | City | State |
---|---|---|---|
Mali | Faculty of Medicine, Pharmacy and Odonto-Stomatology (FMPOS) | Bamako |
Lead Sponsor | Collaborator |
---|---|
National Institute of Allergy and Infectious Diseases (NIAID) |
Mali,
Breman JG, Egan A, Keusch GT. The intolerable burden of malaria: a new look at the numbers. Am J Trop Med Hyg. 2001 Jan-Feb;64(1-2 Suppl):iv-vii. — View Citation
Gupta S, Snow RW, Donnelly CA, Marsh K, Newbold C. Immunity to non-cerebral severe malaria is acquired after one or two infections. Nat Med. 1999 Mar;5(3):340-3. — View Citation
Marsh K, Kinyanjui S. Immune effector mechanisms in malaria. Parasite Immunol. 2006 Jan-Feb;28(1-2):51-60. Review. — View Citation
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