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The efficacy and safety of Conbercept intravitreal injection for choroidal neovascularization secondary of rare macular diseases

The efficacy and safety of Conbercept intravitreal injection for choroidal neovascularization secondary of rare macular diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017495
Enrollment
Unknown
Registered
2018-08-01
Start date
2018-03-31
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

choroidal neovascularization secondary to rare macular diseases

Interventions

Case series:intravitreal Conbercept injections

Sponsors

Zhongshan Ophthalimic Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Be treated with intravitreal Conbercept injections wihtin a month and be willing to join the trial for at least 1 year; 2. Diagnosis of active CNV secondary to rare macular disease after comprehensive examinations; 3. BCVA must be between = 20 and = 83 letters in the study eye; 4. Aged=18 years.

Exclusion criteria

Exclusion criteria: 1. The patients who want to quit the trial; 2. History of intravitreal treatment with steroids/History of laser photocoagulation/History of intraocular treatment with any anti-angiogenic drugs; 3. Women of child-bearing potential; 4. Active malignancies/History of stroke less than 6 months prior to screening/Uncontrolled systemic inflammation or infection; 5. contraindications to fluorescein angiography (FA), ICGA; 6. patients with choroidal neovascularization caused by AMD/pathological myopia/PCV.

Design outcomes

Primary

MeasureTime frame
BCVA;area of CNV;

Countries

China

Contacts

Public ContactWen feng

ZhongShan Ophthalimic Center

wenfeng208@foxmail.com+86 020 87330394

Outcome results

None listed

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