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Intravitreal Conbercept for diabetic macular edema in real-world clinical practice in China: a multi-center, observational study

Intravitreal Conbercept for diabetic macular edema in real-world clinical practice in China: a multi-center, observational study

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064404
Enrollment
Unknown
Registered
2022-10-06
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Diabetic Macular Edema

Interventions

Case series:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years, no gender limit; 2. In patients with type 1 or type 2 diabetes, HbA1c value <=10%; 3. Diagnosed with CIDME; 4. The best corrected visual acuity is within 0.05-0.5 decimal visual acuity; 5. If both eyes met the inclusion criteria, the investigator decided to include a single eye; 6. Agreed to receive Compacept treatment after enrollment; 7. 12 months of follow-up is expected to be completed; 8. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating patients; 2. Intraocular surgery is expected within the next 6 months; 3. History of vitreoretinal surgery, cataract surgery, systemic anti-VEGF therapy and intraocular implant therapy within 6 months prior to treatment; 4. Intraocular anti-VEGF treatment history, ocular hormone use history and panretinal photocoagulation history within 3 months before treatment; 5. The target eye has uncontrollable glaucoma (intraocular pressure >=25mmHg after medical treatment) or a history of glaucoma filtration surgery; 6. Diagnosis or suspected intraocular/periocular infection and inflammation; 7. Serious systemic diseases (such as serious cardiovascular diseases, kidney diseases, etc.) and other eye diseases affect the judgment of the results; 8. Participating in other clinical trials/studies; 9. Other conditions that the researchers determined needed to be excluded.

Design outcomes

Primary

MeasureTime frame
best corrected vision;

Secondary

MeasureTime frame
central subfield thickness;intraretinal fluid;subretinal fluid;cumulative number of injections;adverse event / reaction;

Countries

China

Contacts

Public ContactXu Xun

Shanghai General Hospital

drxuxun@sjtu.edu.cn+86 13386259538

Outcome results

None listed

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