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临床试验/NCT03970161
NCT03970161Unknown不适用

Evaluation of Early Retinal Nerve Injury in Type 2 Diabetes Patients Without Diabetic Retinopathy

Third Affiliated Hospital, Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 720 人开始时间: 2019年5月29日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
720
试验地点
1
主要终点
GCL+ in the macular area obtained using the 3D wide mode

研究概览

简要总结

The object of this study is to investigate the damage to the retinal nerve fiber layer (RNFL) and ganglion cell complex layer (GCL+) in diabetic patients without retinal microangioma as detected by fundus fluorescein angiography (FFA) and to determine the kind of nerve damage more likely to indicate early injury.

详细描述

Patients with type 2 diabetes mellitus and healthy volunteers will be included in our study. Patients with retinal microangioma are excluded by FFA. The parameters around the optic disc and macular area of the above two groups are measured by optical coherence tomography (OCT), and the results will be analyzed using the SPSS 22.0 software.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients with T2DM
  • •Patients without microangioma

排除标准

  • •Patients with any other ocular disease that might affect retinal nerve injury
  • •Patients with optic neuropathy, age-related macular degeneration, retinal and choroidal disease, and retinal artery/vein occlusion.
  • •Patients with hypertension, hematopathy, neuropathy, and other systemic diseases causing retinal nerve changes.
  • •Patients with keratopathy, cataract, and vitreous hemorrhage were also excluded.

研究组 & 干预措施

T2DM Patients

Experimental

Patients without microangioma changes undergoing FFA examination were included in the present study. All of the participants enrolled in the present study underwent a systematic ophthalmic examination.

干预措施: routine ophthalmic examination (Device)

healthy control subjects

Experimental

All of the participants enrolled in the present study underwent a systematic ophthalmic examination.

干预措施: routine ophthalmic examination (Device)

结局指标

主要结局

GCL+ in the macular area obtained using the 3D wide mode

时间窗: 96 weeks

GCL+ in the macular area obtained using the 3D wide mode

RNFL thickness in the macular area obtained using the 3D Macula (v) mode

时间窗: 96 weeks

RNFL thickness in the macular area obtained using the 3D Macula (v) mode

Peripapillary RNFL thickness

时间窗: 96 weeks

Peripapillary RNFL thickness

Retinal thickness in all macular regions

时间窗: 96 weeks

Retinal thickness in all macular regions

GCL+ thickness in the macular region obtained using the 3D Macula (v) mode

时间窗: 96 weeks

GCL+ thickness in the macular region obtained using the 3D Macula (v) mode

次要结局

未报告次要终点

研究者

发起方
Third Affiliated Hospital, Sun Yat-Sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiang Zhu

Professor

Third Affiliated Hospital, Sun Yat-Sen University

研究点 (1)

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