None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy individuals of either sex, aged 1year and above living in same community 2. Informed consent by head of family 3. No symptom of dengue, chikungunya and ILI at the time of enrollment
Exclusion criteria
Exclusion criteria: 1. Symptoms of dengue, chikungunya and ILI/fever in last 7 days at the time of enrolment 2. Pregnant women and lactating mother 3. Child below the age of 1 year 4.Individuals taking other preventive medicines for dengue, chikungunya and Influenza like illness (ILI) 5. Patients with malignancy, immuno-compromised state, life threatening disease, end stage disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in incidence of acute febrile illness between the cohorts at weekly interval.Timepoint: Assessment of the participants every 7 days for 3 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. changes in incidence of dengue & chikungunya fever between the cohorts at weekly interval. 2. Changes in incidence of influenza like illness between the cohorts at weekly interval. 3. Changes in weekly reporting of acute febrile illness between the cohorts. 4. Changes in intensity, duration of acute febrile illness between the cohorts.Timepoint: Assessment of the participants every 7 days for 3 months | — |
Countries
India
Contacts
Central Council for Research in Homoeopathy