About this trial
This study aims to evaluate retinal and choroidal microvascular changes using optical coherence tomography angiography (OCTA) in patients receiving hydroxychloroquine therapy. Hydroxychloroquine is commonly used in the treatment of autoimmune diseases and may cause retinal toxicity with long-term use. OCTA is a non-invasive imaging modality that allows detailed assessment of retinal vascular changes.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Adults (≥18 years old) with documented HCQ therapy for ≥1 year.
Stable systemic disease under medical supervision.
Disqualifiers
-patients with media opacity.
Any pre-existing retinal or optic nerve disease (e.g., diabetic retinopathy, AMD, myopic degeneration).
History of intraocular surgery or trauma.
Uncontrolled systemic vascular diseases (e.g., hypertension)
Trial population
This study includes adults receiving hydroxychloroquine therapy for autoimmune diseases and a control group of healthy volunteers. The aim is to evaluate retinal microvascular changes using OCTA imaging.
Trial design
Cohort
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Superficial Capillary Plexus Vessel Density (SCP)
Measurement of superficial capillary plexus vessel density using optical coherence tomography angiography (OCTA) in patients receiving hydroxychloroquine therapy.
Deep Capillary Plexus Vessel Density (DCP)
Measurement of deep capillary plexus vessel density using optical coherence tomography angiography (OCTA) in patients receiving hydroxychloroquine therapy.
Locations
Sponsors and contacts
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