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Prospective clinical study on the efficacy and safety of Intra-arterial therapy in nonarteriotic anterior ischemic optic neuropathy

Prospective clinical study on the efficacy and safety of Intra-arterial therapy in nonarteriotic anterior ischemic optic neuropathy

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081505
Enrollment
Unknown
Registered
2024-03-04
Start date
2024-06-07
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Nonarteriotic anterior ischemic optic neuropathy

Interventions

Intra-arterial treatment:Ophthalmic-artery superselective therapy

Sponsors

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Patients clinically diagnosed with unilateral non-arterial ischemic optic neuropathy within 1 month (2) Age between 40 and 70 (3) BCVA=0.1 (4) Voluntarily participate in the clinical trial and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients diagnosed with bilateral NAION. (2) Patients with features of arterial ischemic optic neuropathy: CRP>10mg/L, Erythrocyte sedimentation rate > ULN ( Male 15mm/h, Female 20mm/h) (3) Coagulation function: International Normalized ratio (INR) > 1.4, and activated partial thromboplastin time (APTT) > 34s. (4) Blood routine examination: Absolute value of peripheral blood neutrophils (ANC) 1.5 x ULN (normal upper limit 17.1µmol/L); Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) > 5 x ULN (normal upper limit 40U/L); Albumin < 20 g/L. (6) Renal function: serum creatinine (Scr) was greater than the maximum reference concentration (Male 1.7 mg/dL, Female 1.4 mg/dL). (7) Any conditions that the researchers consider necessary to exclude from the study.

Design outcomes

Primary

MeasureTime frame
Visual field index;

Secondary

MeasureTime frame
Best-corrected visual acuity;Improvement rate of papilledema;Improvement rate of macular retinal edema;Retinal nerve fibre layer thickness (RNFL);

Countries

China

Contacts

Public ContactXuyang Wen

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine

winston-a@hotmail.com+86 21 6313 5606

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026