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Clinical observation of conbercept in treatment of w-AMD and changes in serum VEGF-related protein levels

Clinical observation of conbercept in treatment of w-AMD and changes in serum VEGF-related protein levels

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100053627
Enrollment
Unknown
Registered
2021-11-26
Start date
2021-12-01
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Wet age-related macular degeneration

Interventions

3+PRN group:Initially, the drug was administered once a month, followed up every month after 3 consecutive times, and treated as needed
T&E group:Initially, the drug was administered once a month, followed up every month after three consecutive times until the retinal exudation was controlled, and then the interval of the next follow-

Sponsors

Xi'an NO.1 Hospital (The First Affiliated Hospital of Northwestern University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients diagnosed with w-AMD, aged >= 50 years, regardless of gender; 2.Patients can sign informed consent for treatment and can follow up according to the agreement of clinical research; 3.Best Corrected Vision (ETDRS): (1) 19 letters <= BCVA <= 73 letters (equivalent to Snellen visual acuity: 20/400 <= BCVA <= 20/40), intraocular pressure (IOP) <= 21mmHg; (2) OCTA examination indicated choroidal neovascularization and exudation between retinal layers; (3) ICGA/FFA indicated choroidal neovascularization and fluorescein leakage. 4.Patients who are willing to sign informed consent and can follow up for a long time.

Exclusion criteria

Exclusion criteria: 1.There are eyelid ectropion, conjunctivitis, keratitis, dacryocystitis and other ocular surface diseases; 2.Received intravitreal, periocular or systemic anti VEGF or cortical sterol treatment within 6 months; 3.The target eye underwent intraocular or periocular surgery and received PDT and retinal laser photocoagulation within 6 months; 4.The target eye has other eye diseases and diseases affecting BCVA or is taking oral drugs affecting BCVA; 5.Patients with poor blood glucose control and poorly controlled blood pressure; 6.Patients with a history of myocardial infarction or cerebral infarction; There are confirmed systemic immune diseases or other systemic diseases such as AIDS, active hepatitis, severe mental, neurological, cardiovascular, respiratory diseases, etc.

Design outcomes

Primary

MeasureTime frame
Best-corrected visual acuity (BCVA);Thickness of central retina of macula;Area of neovascular;Vascular endothelial growth factor-related protein;

Secondary

MeasureTime frame
Macular pigment density;Intraocular pressure;

Countries

China

Contacts

Public ContactChen Xiaodong

Xi'an NO.1 Hospital (The First Affiliated Hospital of Northwestern University)

390203850@qq.com+86 15667058809

Outcome results

None listed

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