Hydroxychloroquine Retinopathy

3

Review clinical trials related to Hydroxychloroquine Retinopathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Adaptive Optics Imaging of Outer Retinal Diseases

The objective of the study is to collect adaptive optics (AO) retinal images from human subjects with outer retinal diseases (diseases of the outer retina including photoreceptor, retinal pigment epithelium (RPE), basement membrane or choroidal pathologies) to develop new diagnostic methods, biomarkers, and clinical endpoints.

Participants needed: 100
Trial details
Age: 21+Biological sex: AllType: ObservationalSponsor: Food and Drug Administration (FDA)Updated: May 8, 2026Locations: 2
Eligibility criteria

Are 21 years of age or older, [+3]

Have a condition which prevents adequate images from being obtained (e.g. unstab... [+4]

Status: Not yet recruiting

Optical Coherence Tomography Angiography Evaluation Of Patients Taking Hydroxychloroquine

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.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Sohag UniversityUpdated: Feb 13, 2026
Eligibility criteria

Adults (≥18 years old) with documented HCQ therapy for ≥1 year. [+1]

-patients with media opacity. [+3]

Status: Recruiting

Novel ERG for Detection of Hydroxychloroquine Retinopathy

The purpose of the study is to investigate novel electroretinography (ERG) devices in the detection of hydroxychloroquine retinopathy. Two devices (the RETEval full-field and flicker ERG and UTAS multifocal ERG) will be evaluated in this study, comparing device outputs to standard of care screening tests, in groups of participants characterised by presence or absence of hydroxychloroquine-related retinopathy.

Participants needed: 140
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: King's College Hospital NHS TrustUpdated: Aug 6, 2025Locations: 1
Eligibility criteria

Age ≥18 years [+1]

Cataract grade ≥3 of any subtype [+18]