Health Condition 1: H158- Other disorders of sclera
Conditions
Interventions
Intervention1: NIL OBSERVATIONAL: NIL OBSERVATIONAL
Sponsors
Biotechnology Industry Research Assistance Council
Eligibility
Inclusion criteria
Inclusion criteria: Patients with any type of uveitis who visits the department of Ophthalmology
Exclusion criteria
Exclusion criteria: Any subject who cannot come for further consultations following baseline work up. Intraocular surgery in the 3 months previous to enrollment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of the study is to develop a multi centric registry for uveitis diseases to understand epidemiology & treatment pattern of uveitis and to evaluate the health economics involved in the treatment of uveitis in different geographical regions in India. Timepoint: 1month to 10months | — |
Secondary
| Measure | Time frame |
|---|---|
| To collect data of demographics, clinical history & presentations, investigation of uveitis to identify the burden and pattern of uveitis and its treatment in different geographical regions across India. To evaluate the changes in clinical profile and investigational parameters between baseline and follow-up visits. To facilitate the recruitment for future clinical trials in the area of medical uvea diseases by identifying potential participants interested in research.To understand the impact of Covid-19 in patients with uveitis. Timepoint: 6 Months | — |
Countries
India
Contacts
Public ContactDrMerin Dciskon
Amrita Institute of Medical science
Outcome results
None listed