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To observe the stability of stable nAMD patients treated with PRN and T&E protocol of anti-VEGF treatment when they recovered from discontinued treatment affected by COVID-19 outbreak

To observe the stability of stable nAMD patients treated with PRN and T&E protocol of anti-VEGF treatment when they recovered from discontinued treatment affected by COVID-19 outbreak

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100046164
Enrollment
Unknown
Registered
2021-05-07
Start date
2018-07-01
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

neovascular age-related macular degeneration

Interventions

T&E Group:Nil
PRN group:Nil

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as monocular or binocular nAMD, BCVA is 0.05-0.5 (23-73 letters); 2. Before the COVID-19 epidemic, the patient received intravitreal injection of arbacicept treatment with 3+T&E, or 3+PRN therapeutic regime; 3. During the epidemic period, there was no follow-up and no treatment; 4. After the end of the epidemic, continue to treat and follow-up in our hospital; 5. The last follow-up showed that the disease was stable as follows: (1) The best corrected visual acuity lost no more than 5 letters (or one line) compared with the previous follow-up; (2) The CRT increased by no more than 10% compared with the previous follow-up; (3) OCT showed no obvious increase of effusion compared with the previous follow-up; (4) OCT showed no obvious new effusion; (5) No obvious new haemorrhage; (6) No new CNV on octa.

Exclusion criteria

Exclusion criteria: 1.New CNV or CME caused by other reasons; 2.Patients has been treated with laser, PDT and other treatments in the past; 3.Patients who had received anti-VEGF treatment in the study eye or contralateral eye in the past 3 months; 4.Patients with neovascularization of anterior segment (including iris and angle) or neovascular glaucoma; 5.The study eyes had undergone vitreoretinal surgery and / or scleral buckling; 6.Patients who were not treated and followed up according to the specified treatment plan.

Design outcomes

Primary

MeasureTime frame
Central retinal thickness;

Secondary

MeasureTime frame
Best corrected visual acuity;subretinal fluid;intraretinal fluid;subretinal hyperreflective material;choroidal neovascularization;subretinal choroidal thickness;

Countries

China

Contacts

Public ContactSun Dawei

Department of Ophthalmology, Second Affiliated Hospital of Harbin Medical University

drsundw@126.com+86 13304505525

Outcome results

None listed

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