Skip to content

A Study on the Safety and Efficacy of Thrombolytic Therapy for Acute Non-arteritic Central Retinal Artery Occlusion

A Study on the Safety and Efficacy of Thrombolytic Therapy for Acute Non-arteritic Central Retinal Artery Occlusion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127638
Enrollment
Unknown
Registered
2026-07-03
Start date
2026-07-03
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-arteritic central retinal artery occlusion (NA-CRAO)

Interventions

Neurology Thrombolytic Therapy Team:Intravascular thrombolysis
Routine ophthalmic treatment group:conventional treatment

Sponsors

The First Affiliated Hospital of USTC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Definite diagnosis of non-arteritic central retinal artery occlusion by fundus findings and/or OCT; 2.Initial visual acuity = 0.1; 3.Age = 18 years; 4.Time from onset = 24 hours; 5.Signed informed consent from the patient and family;

Exclusion criteria

Exclusion criteria: 1.Fundus examination revealed no definite embolic site in the retinal artery, and macular OCT showed non-inner retinal edema. 2.Arteritic CRAO (central retinal artery occlusion) or giant cell arteritis; 3.Pre-existing blinding eye disease; after evaluation and treatment, visual function remains at the level of blindness; 4.Branch retinal artery occlusion, combined with central retinal artery and vein occlusion, proliferative diabetic retinopathy, ocular hypertension, and suspected ophthalmic artery occlusion. 5.CRAO related to facial cosmetic fillers; 6.MRI/CT revealed intracranial hemorrhage; 7.History of acute coronary syndrome, myocardial infarction, coronary revascularization, cerebrovascular accident, or transient ischemic attack within the last 6 months. 8.Subject has medical or psychiatric illness, or any condition that could compromise the subject's health or could interfere with, limit, or confound the protocol-defined assessments. 9.Presence of an active systemic infection. 10.Systemic issues including uncontrolled blood pressure and blood glucose that may compromise thrombolytic therapy. 11.Inability to attend or comply with follow-up visits; 12.Pregnant women (confirmed by HCG); 13.Current use of oral anticoagulants such as warfarin, or treatment with heparin within the past 48 hours. 14.History of surgery, biopsy, or significant trauma within the last 2 months. 15.Presence of severe hepatic and renal impairment, pancreatitis, or active peptic ulcer disease. 16. There is cognitive impairment, with a Mini-Mental State Examination (MMSE) score of less than 27.

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuity;

Secondary

MeasureTime frame
central macular thickness;

Countries

China

Contacts

Public ContactYonghao Gu

The First Affiliated Hospital of USTC

aerolplane@hotmail.com+86 551 6228 4043

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026