None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Voluntary written informed consent by the family head
Exclusion criteria
Exclusion criteria: Pregnant women and lactating mother Child below age of 1 year Individuals taking other preventive medicines for dengue. Patients with malignancy, immune-compromised state, life threatening diseases, end stage diseases. Symptom of acute febrile illness/ Dengue like illness at the time of enrolment. Patient with symptoms of acute infectious illnesses at the time of enrolment. Not willing to give written informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence of Dengue between the groupsTimepoint: Weekly | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence of AUFI between the groupsTimepoint: Weekly;Changes/severity of symptoms between the groups during post prophylactic/ climatic infectionsTimepoint: at the time of analysis;Mean duration of acute febrile illnesses between the cohortsTimepoint: Weekly | — |
Countries
India
Contacts
Central Council for Research in Homoeopathy