Central Retinal Artery Occlusion

2

Review clinical trials related to Central Retinal Artery Occlusion. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Microneedle Intra-Arterial Injection for Retinal Artery Occlusion

This prospective interventional study evaluates the efficacy and safety of direct intra-arterial microneedle injection combined with pars plana vitrectomy for acute retinal artery occlusion (including central retinal artery occlusion \[CRAO\] and branch retinal artery occlusion \[BRAO\] involving the macula or causing severe visual loss). The primary endpoint is best-corrected visual acuity (BCVA, LogMAR) at 1 month. Secondary objectives include assessing the effect of treatment timing and monitoring longitudinal changes in visual function and retinal structure over 12 months.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Second Affiliated Hospital, School of Medicine, Zhejiang UniversityUpdated: Sep 3, 2025Locations: 1
Eligibility criteria

Age ≥18 years [+2]

Active bleeding disorder, or significant bleeding within the past 3 months, or b... [+9]

Status: Recruiting

Visual Involvement in Giant Cell Arteritis

This observational study aims to enhance the description of the different ways Giant Cell Arteritis (GCA) affects vision. The latest technology and knowledge are used to improve how we diagnose and predict patient outcomes. GCA is the most frequent vasculitis, an inflammation of vessels, in older adults. It involves large and medium-sized arteries and causes ischemic alterations such as stroke and blindness, through damage of extracranial arteries. The primary objective is to compare the frequency of the various ocular findings between the main alterations of arteritic and non-arteritic aetiology, such as Arteritic Anterior Ischemic Optic Neuropathy (A-AION) Vs. Non-Arteritic Anterior Ischemic Optic Neuropathy (NA-AION) or Central Retinal Artery Occlusion (CRAO) from GCA Vs. from other causes, through a comprehensive clinical and instrumental evaluation.

Participants needed: 762
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: ASST Fatebenefratelli SaccoUpdated: Jul 15, 2024Locations: 1
Eligibility criteria

Patients older than 18 years with clinically suspected or confirmed gigantocellu... [+4]

Pre-existing ophthalmological pathologies that may modify best visual acuity and... [+3]