None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Study will be carried out in individuals above 2 Years of age. 2.Individuals currently residing and likely to stay till the end of one year in the study area. 3.Consented to participate in both sections of the study (Sero Prevalence and AFI Surveillance) and follow all study procedures.
Exclusion criteria
Exclusion criteria: Ongoing fever episodes or history of AFI on or within 3 calendar days before enrolment for the cohort
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome is estimation of the burden of diseases causing acute febrile illness with focus on Dengue & Chikungunya at community level & determine the seasonal variations and the rate of transmission in the incidence of acute febrile illnessesTimepoint: Baseline and at the end of 12 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.The identification of groups who are most vulnerable to Dengue & Chikungunya infection (e.g. age groups, gender, occupation) 2.The sensitivity and specificity of IgG ELISA will be calculated against PRNT (Neutralizing antibodies). 3.The cost of illness of a case of dengue fever, chikungunya fever and dengue hemorrhagic fever will be calculated for both hospitalized and ambulatory cases Timepoint: all secondary outcomes will be assessed at the end of one year from baseline | — |
Countries
India
Contacts
MediCiti Institute of Medical Sciences