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Evaluation of the efficacy of Conbercept in the treatment of diabetic macular edema based on OCTA

Evaluation of the efficacy of Conbercept in the treatment of diabetic macular edema based on OCTA

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032728
Enrollment
Unknown
Registered
2020-05-08
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-05-11

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

Conditions

Diabetic macular edema

Interventions

Group 1:3+PRN (pro re nata)
Group 2:6+PRN(pro re nata)

Sponsors

Inner Mongolia Chaoju Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. The patients who know about the study and sign the informed consent and are willing to perform according to the requirements of the clinical trial scheme; 2. The patients who meet the diagnostic criteria of type 2 diabetes issued by who are between 30 and 80 years old; 3. Patients who meet the criteria of non proliferative phase and diabetic macular edema recommended by American ophthalmic society and international ophthalmic society in 2003; 4. In patients with macular edema by OCT, the thickness of macular central area with a diameter of 1 m m was >= 300 µ M; 5. The best corrected visual acuity letter score of ETDRS is 78-24 (20 / 32-20 / 320); 6. Without macular grid photocoagulation, intravitreal injection of triamcinolone acetonide and intravitreal injection of anti VEGF drugs.

Exclusion criteria

Exclusion criteria: 1. The patients whose refractive stroma is turbid, which affects the observation of fundus; 2. Patients with glaucoma, retinal vein occlusion, uveitis, optic nerve disease and other fundus diseases; 3. The general condition is not good, the patients with severe cardiovascular, cerebrovascular, liver and hematopoietic diseases, diabetic nephropathy with renal failure, and the patients with serious life-threatening primary diseases and psychosis; 4. Pregnant or lactating women; 5. Patients who are participating in clinical trials of other drugs; 6. Patients who are unable to cooperate with each examination due to age, disease and other reasons.

Design outcomes

Primary

MeasureTime frame
BCVA;CMT;Blood flow density;

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 17, 2026