Health Condition 1: H358- Other specified retinal disorders
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants aged 50 years and above attending the ophthalmology outpatient department during the study period and diagnosed with the condition under study will be eligible for inclusion. Patients who are willing to undergo detailed ophthalmic examination and retinal imaging including Optical Coherence Tomography and Fundus Fluorescein Angiography where indicated, and who provide written informed consent to participate in the study will be included.
Exclusion criteria
Exclusion criteria: Patients who refuse to provide informed consent or are unable to cooperate with ocular examination will be excluded. Patients with significant media opacity preventing adequate retinal imaging, a history of recent ocular surgery or trauma, or the presence of other retinal or ocular diseases that may confound the study findings will also be excluded. In addition, patients with known contraindications to fluorescein dye used in fundus fluorescein angiography will not be included in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of retinal microvascular changes using Optical coherence tomography and Fundus fluorescein angiographyTimepoint: At baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| Association of demographic & lifestyle risk factors (age, smoking, tobacco use, sunlight exposure, BMI & systemic diseases) with AMD.Timepoint: At baseline;Association of retinal findings with clinical parametersTimepoint: At baseline;Correlation with laboratory parametersTimepoint: At baseline | — |
Countries
India
Contacts
Jawaharlal Nehru Medical College