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Anti-VEGF combined with macular photocoagulation therapy for the treatment of advanced-stage exudative age-related macular degeneration

Anti-VEGF combined with macular photocoagulation therapy for the treatment of advanced-stage exudative age-related macular degeneration

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046139
Enrollment
Unknown
Registered
2021-05-05
Start date
2021-06-01
Completion date
Unknown
Last updated
2021-12-21

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

Conditions

exudative age-related macular degeneration

Interventions

experimental group:Accurate macular photocoagulation combined with intravitreal injection of anti-VEGF

Sponsors

Hainan Hospital of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=45 years; 2. The patient was diagnosed as wet-type AMD (including CNV, PCV) in our hospital after relevant examination (slit lamp, fundus photography, Oct, ERG, FFA, ICGA, etc.) and combined with clinical diagnosis; 3. The position of choroidal neovascularization is located 500um outside the center of fovea; 4. The best corrected visual acuity of ETDRS was 0-73 letters; 5. The target eyes were treated with anti VEGF 3 times or more before the experiment, and there was no refractive media turbidity and pupil reduction that affected fundus examination; 6. Sign the informed consent form and be willing to follow up according to the protocol.

Exclusion criteria

Exclusion criteria: 1. Subjects who voluntarily quit; 2. The area of bleeding or exudation in the target eye was more than 6 optic discs; 3. The diameter of scar or fibrosis in the paraocular fovea was more than 500 um; 4. The target eye is associated with other eye diseases (such as RVO, Rao, Dr, DME, CSC, etc.), excluding pathological myopia, cataract and other factors affecting refractive media; 5. There are diseases or conditions in the target eye or the whole body that the researchers think if the subjects continue to participate in this study, they may face greater risks (such as vitrectomy history, grade 3 hypertension, AIDS, malignant tumor, serious mental, cardiovascular, neurological, respiratory, digestive and other system diseases, or long-term hormone use, immune deficiency disease, heart stent surgery, organ poor blood glucose control in diabetic patients; 6. The target eye has undergone intraocular or periocular surgery within 3 months (including laser photocoagulation near the central fovea, cataract surgery, etc.), except for the eyelid surgery which does not affect the vitreous injection (but the eyelid surgery cannot be performed within one month before the administration); 7. The target eye had received corneal transplantation; 9. Cardiovascular events such as stroke, cerebral ischemia and myocardial infarction occurred in the first 6 months; 10. Those who do not use effective contraception; 11. In the course of the study, the researcher decided that it was not suitable to continue to participate in the experiment.

Design outcomes

Primary

MeasureTime frame
improvement rate of visual acuity;

Secondary

MeasureTime frame
Macular thickness;Area of choroidal neovascular lesions;

Countries

China

Contacts

Public ContactHuang Houbin

Hainan Hospital of PLA General Hospital

huanghoubin@hotmail.com.cn+86 15692537817

Outcome results

None listed

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