Skip to content

A clinical study for conbercept in neovascular glaucoma patients

A clinical study for conbercept in neovascular glaucoma patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019918
Enrollment
Unknown
Registered
2018-12-08
Start date
2015-05-27
Completion date
Unknown
Last updated
2018-12-10

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

Conditions

neovascular glaucoma

Interventions

Case series:intravitreal conbercept

Sponsors

Tianjin Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 82 Years

Inclusion criteria

Inclusion criteria: 1. patients whose underlying diseases were DR, CRVO, carotid artery stenosis or occlusive disease; 2. patients who did not have PRP before; 3. patients who were 18 to 85 years old; 4. patients who underwent intravitreal injection with a visual acuity = hand motion, or the visual acuity of patients with enucleation had no light perception; 5. patients with an IOP >21 mmHg and under the maximum dose of antiglaucoma medications; 6. patients with iris or angle neovascularization; 7. patients with or without pupillary pigment epithelium.

Exclusion criteria

Exclusion criteria: 1. NVG combined with ocular tumours or uveitis; 2. severe cardiovascular and cerebrovascular diseases; 3. patients who had recent active inflammation of the eye; 4. patients who failed to complete the scheduled follow-ups for various reasons.

Design outcomes

Primary

MeasureTime frame
Best-corrected visual acuity;Intraocular pressure;anti-glaucoma medications;Vascular endothelial growth factor;Transforming growth factor-ß1;Placenta growth factor;Histopathological analysis of trabeculectomy specimens;Postoperative complications;

Countries

China

Contacts

Public ContactJin Yang

Tianjin Eye Hospital

yangjin979@163.com+86 13820873540

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 2, 2026