Helminth and malaria parasitic diseases Infections and Infestations
Conditions
Interventions
400 mg albendazole (oral) or matching placebo every three months for 2 years.
Sponsors
Royal Netherlands Academy of Arts and Sciences (Netherlands)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Both males and females 2. Age >=2 years. No upper age limit. 3. Those who have given informed consent
Exclusion criteria
Exclusion criteria: 1. History of chronic liver, heart or central nervous system (CNS) disease 2. Allergy to albendazole
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Prevalence of malaria parasite, assessed throughout the study for 3 years 2. Infection with intestinal helminth before treatment and within 1, 2 and 3 years after start of treatment 3. Skin reactivity to allergens assessed before treatment and within 1, 2 and 3 years after start of treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Immune response to malaria and helminth antigens, assessed before albendazole treatment and within 1, 2 and 3 years after the start of treatment (with the last treatment given at least 2 months before immunological determination). | — |
Countries
Indonesia
Outcome results
None listed