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A randomized controlled trial for intravitreal injection of Anti-VEGF and post-sclera injection of triamcinolone acetonide in the treatment of punctate inner choroidopathy (PIC) complicated with choroidal neovascularization

A randomized controlled trial for intravitreal injection of Anti-VEGF and post-sclera injection of triamcinolone acetonide in the treatment of punctate inner choroidopathy (PIC) complicated with choroidal neovascularization

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017555
Enrollment
Unknown
Registered
2018-08-03
Start date
2018-08-01
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

punctate inner choroidopathy (PIC) complicated with choroidal neovascularization

Interventions

1:intravitreal injection of Anti-VEGF
2:intravitreal injection of Anti-VEGF and post-sclera injection of triamcinolone acetonide

Sponsors

Southwest Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 to 65 years who have signed informed consent for the clinical trial; 2. Diagnosing PIC with CNV: The posterior pole conforms to the pathological manifestations of PIC, fluorescein angiography (FA) is found to have CNV leakage, and optical coherence tomography (OCT) is found to have intraretinal or subretinal fluid or central retinal thickness (CRT) Increased; 3. At least one of the following types of CNV lesions involving the central macular area: central fovea; near fovea; central fovea; optic disc margin (abnormal neovascularization around the optic papilla) and involving the central region of the macula; 4. Study eye BCVA = 24 letters and = 86 letters (approximately equal to 20 / 320 to 20 / 25 of Snellen's eye chart); 5. Visual loss must be caused only by the above type of CNV of PIC.

Exclusion criteria

Exclusion criteria: 1. Systemic history and conditions: (1) uncontrollable hypertension (>140/90 mmHg); (2) hypersensitivity; (3) history of stroke or myocardial infarction within 3 months; (4) use of other studies within 30 days Drugs; (5) use systemic glucocorticoids or anti-VEGF drugs within 6 months; (6) use systemic drugs known to be toxic to the lens, retina or optic nerve, including deferoxamine, chloroquine/hydroxychloroquine,tamoxifen, phenothiazine and ethambutol; (7)women patients who are in pregnancy or lactation period. 2. Eye history and conditions (both eyes): (1) any active eye infection; (2) active intraocular inflammation; (3) iris neovascularization or neovascular glaucoma; (4) history of uveitis; ) vitreous macular traction syndrome; (5) unable to obtain a sufficient quality fundus photograph or fluorescein angiography for analysis; (6) unilateral or contralateral BCVA: ETDRS = 24 letters; (7) use any within 3 months Hormone and anti-angiogenic drugs (including any glucocorticoids and anti-VEGF drugs) 3.Eye history and conditions (study eye): (1) uncontrollable high intraocular pressure (IOP = 24 mmHg); (2) glaucoma (cup to disk ratio = 0.8); (3) any confusion of interpretation of the results of the study, damage to vision, Ophthalmic diseases or treatments requiring medication or surgery, including cataracts, retinal vascular occlusion, retinal detachment, macular hole or choroidal neovascularization; (4) structural damage within 0.5 disc diameter from the center of the macula; (5) Combined with AMD, PCV; (6) laser photocoagulation within 3 months; (7) intraocular surgery within 3 months; (8) 6 months, intravitreal injection of hormone therapy; 3 months, eye sugar History of treatment with corticosteroids; (9) intravitreal injection of anti-VEGF drugs within 3 months; (10) history of vitrectomy; (11) CNV caused by pathological myopia; (12) other requirements associated with glucocorticoid therapy Eye condition.

Design outcomes

Primary

MeasureTime frame
Macular thickness;ETDRs;

Countries

China

Contacts

Public ContactLi Shiying

Dept. Ophthalmology, Southwest Hospital

shiying_li@126.com+86 13648430819

Outcome results

None listed

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