About this trial
This study aims to:
1. To evaluate the effectiveness of Immulant ® addition to standard treatment in reducing clinical symptoms of Cryptosporidiosis in immunocompromised children. 2. To measure the changes in parasite count in stool samples after treatment with Immulant ®. 3. To assess the safety and tolerability of Immulant ® in children participating in the study.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Clinical diagnosis of Cryptosporidiosis Disease
Age from 5-12 years
Immunocompromised children
Not receiving any drugs causing immunosuppression
Disqualifiers
Patients undergoing organ transplantation
Patients suffering from autoimmune diseases.
Patients suffering from hypersensitivity of this plant extract
Trial design
Single group
Treatments tested in this trial
Echinacea Extract
DrugImmulant ® (an extract derived from Echinacea purpurea plant)
Treatment groups
Trial outcomes
Primary outcomes
To measure the changes in parasite count in stool samples after treatment
Sponsors and contacts
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