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To observe the curative effect of Conbercept in the treatment of macular disease in Mongolian population:A multicenter self controlled study

To observe the curative effect of Conbercept in the treatment of macular disease in Mongolian population:A multicenter self controlled study

Status
Recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062369
Enrollment
Unknown
Registered
2022-08-02
Start date
2022-08-01
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

macular disease(DME?AMD?CNV)

Interventions

Mongolian group:Three & PRN
Han group:Three & PRN

Sponsors

Inner Mongolia Chaoju Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Aged over 18 years old; (2) The patients were informed about the study and signed the informed consent form, and they were willing and carried out in accordance with the requirements of the clinical trial protocol; (3) Diabetic patients meet the diagnostic criteria for type 2 diabetes promulgated by WHO; (4) Meet the non-proliferative diagnostic criteria for diabetic retinopathy recommended by the American Academy of Ophthalmology and the International Academy of Ophthalmology in 2003, and meet the diagnostic criteria for diabetic macular edema; (5) Patients diagnosed with (wAMD containing PCV, DME, CNV) after fundus color photography, OCT/OCTA, FFA/ICGA examination; (6) BCVA is 0.05-0.5 (including 0.05 and 0.5); (7) There is macular edema in the OCT/OCTA examination, and the thickness of the central macular area within 1 mm in diameter is >=300 µm; (8) Nationality is determined by ID card registration.

Exclusion criteria

Exclusion criteria: (1) Severe refractive interstitial opacity, affecting the fundus observer; (2) Patients with fundus diseases such as glaucoma, retinal vein occlusion, uveitis, optic nerve disease; (3) Patients with poor general condition, serious cardiovascular and cerebrovascular, liver and hematopoietic diseases, diabetic nephropathy and renal failure, serious life-threatening primary diseases and mental illness; (4) Pregnant or lactating women (contraception during the study); (5) Those who are participating in clinical trials of other drugs; (6) Those who are unable to cooperate in completing various inspections due to age, disease, etc.; (7) Patients with poor compliance; (8) Received anti-VEGF or hormone therapy within 3 months; (9) Patients who have received retinal photocoagulation within 3 months.

Design outcomes

Primary

MeasureTime frame
General patient information;BCVA;CMT;NEI VFQ-25;Biochemical Indicators;IOP;

Secondary

MeasureTime frame
deep blood flow density;superficial blood flow density;Area of FAZ;Perimeter of FAZ;Complication;

Countries

China

Contacts

Public ContactZhang Guisen

Inner Mongolia Chaoju Eye Hospital

zhangguisen76@sohu.com+86 18904719852

Outcome results

None listed

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