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Clinical Trial Summary

Eyes with diabetic macular edema requiring conbercept treatment will be followed up for one month. Before treatment, one week after treatment and one month after treatment, the eyes will be examined by optical coherence tomography (OCT) and optical coherence tomographic angiography (OCTA). The changes of macular edema will be observed and analyzed by OCT leakage mapping software, and the relationship between the changes of macular edema and visual acuity will be analyzed.


Clinical Trial Description

1. Research purpose:

After one month follow-up, we will observe whether OCTleakage mapping can be used as a biomarker to predict the prognosis of DME eyes, and will observe the effect of Conbercept on improving edema and visual acuity of DME eyes.

2. Subjects Number of subjects planned to be recruited: 35

Inclusion criteria:

1. Age ≥ 18

2. Diabetic macular edema eyes treated with conbercept for the first time in 1 week

3. Informed consent of patients and signing of informed consent

Exclusion criteria:

1. High myopia

2. Macular diseases affecting vision

3. Vitreous hemorrhage requiring surgery

4. Patients with anterior segment neovascularization

5. Eye or periocular infection

6. Optic neuropathy and glaucoma

7. Periphlebitis, ophthalmic ischemic syndrome, uveitis, coat's disease, FEVR and other retinal diseases

8. Ametropia and cataract surgery

9. In 3 months, in addition to this treatment of conbercept, other anti VEGF treatment, laser treatment or vitreoretinal surgery were performed

10. Other systemic diseases can not complete follow-up ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04254536
Study type Observational
Source Renmin Hospital of Wuhan University
Contact Hongmei Zheng, MD
Phone +86 13871484442
Email 13871484442@139.com
Status Not yet recruiting
Phase
Start date February 1, 2020
Completion date December 31, 2020

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