Toxocariasis Clinical Trial
Official title:
Treatment of Asymptomatic Toxocariasis With Albendazole in Children. A Prospective, Randomized, Placebo-controlled Clinical Trial
| Verified date | February 2023 |
| Source | Hospital de Niños R. Gutierrez de Buenos Aires |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to evaluate effectiveness of albendazole in the treatment of the asymptomatic infection with the parasite Toxocara in children. Treatment response is defined as a reduction in the number of eosinophils in blood. The study drug will be compared to placebo and randomly assigned in a double blind manner. Follow up will be prospective. 50 children (25 per group) will be enrolled in the study.
| Status | Active, not recruiting |
| Enrollment | 45 |
| Est. completion date | July 2025 |
| Est. primary completion date | July 2015 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 2 Years to 15 Years |
| Eligibility | Inclusion Criteria: - Pediatric ambulatory patients with asymptomatic toxocariasis - Children 2 - 15 years old - Absolute eosinophil count > 1100 / mm3 - Normal ophthalmoscopy Exclusion Criteria: - Treatment with a benzimidazole in the previous year - Infection by other nematodes (Ascaris lumbricoides, strongyloides stercoralis, uncinarias, Trichuris trichuria) - Symptomatic patients (prolonged fever, acute pneumonitis, hepatomegaly, splenomegaly, ocular compromise due to toxocara) - Concomitant diseases - Immunocompromised patients - Altered liver or kidney function - Pregnancy |
| Country | Name | City | State |
|---|---|---|---|
| Argentina | Parasitology Division, Children's Hospital "R Gutierrez" of Buenos Aires | Buenos Aires |
| Lead Sponsor | Collaborator |
|---|---|
| Hospital de Niños R. Gutierrez de Buenos Aires |
Argentina,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Mean absolute reduction in eosinophil count from baseline | 12 months after treatment | ||
| Secondary | Reduction in eosinophil count in more than 60% from baseline | 1 year | ||
| Secondary | Incidence of adverse drug events | 3, 6, 9 and 12 months after treatment | ||
| Secondary | Mean absolute reduction in eosinophil count | 3, 6, 9 months after treatment |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Recruiting |
NCT03814837 -
A Study for the Ocular Toxocariasis Patients With the Pulmonary Toxocariasis, and Ocular Toxocariasis Cohort
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