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临床试验/NCT02581995
NCT02581995已完成4 期

Open-label Phase-4 Study to Examine the Change of Vision-related Quality of Life in Subjects With Diabetic Macular Edema (DME) During Treatment With Intravitreal Injections of 2 mg Aflibercept According to EU Label for the First Year of Treatment

Bayer0 个研究点目标入组 560 人开始时间: 2015年11月19日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
Bayer
入组人数
560
主要终点
Change From Baseline to Week 52 in NEI VFQ-25 Total Score

研究概览

简要总结

To evaluate the change in quality of life (NEI VFQ 25) in subjects with DME during the first year of treatment with aflibercept according to the EU Label.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Type 1 or 2 diabetes mellitus
  • Diagnosis of DME secondary to diabetes mellitus involving the center of the macula (defined as the area of the center subfield on OCT) in the study eye
  • Decrease in vision determined to be primarily the result of DME in the study eye
  • BCVA in the study eye of ETDRS letter score 73 to 24 (This corresponds to a Snellen equivalent of approximately 20/40 to 20/320.)

排除标准

  • Pregnancy and lactation
  • Mismatch with inclusion criteria

研究组 & 干预措施

Arm 1 / Quality of Life

Experimental

Aflibercept treatment in subjects with diabetic macular edema (DME)

干预措施: Eylea (Aflibercept, VEGF Trap-Eye, BAY86-5321) (Drug)

结局指标

主要结局

Change From Baseline to Week 52 in NEI VFQ-25 Total Score

时间窗: Baseline, Week 52

National eye institute 25-item visual function questionnaire (NEI VFQ-25) is a condition-specific measure which was designed to capture the specific impact of vision loss on health-related quality of life (HRQoL). The calculation for NEI VFQ-25 sub-scale scores and total score was performed according to the "NEI VFQ-25 Scoring Algorithm - August 2000". The NEI VFQ-25 consists of a base set of 25 vision-targeted questions representing 11 vision-related constructs, plus an additional single-item general health rating question. All items are scored so that a high score represents better functioning. Each item is then converted to a 0 to 100 scale so that the lowest and highest possible scores are set at 0 and 100 points, respectively. In this format scores represent the achieved percentage of the total possible score, e.g. a score of 50 represents 50% of the highest possible score.

次要结局

  • Change From Baseline to Week 52 in Central Retinal Thickness (CRT) Measured by Optical Coherence Tomography (OCT)(Baseline, Week 52)
  • Change From Baseline to Week 52 in the NEI VFQ 25 Near Activities Subscale(Baseline, Week 52)
  • Change From Baseline to Week 52 in the NEI VFQ 25 Distant Activities Subscale(Baseline, Week 52)
  • Proportion of Participants Progressing to Greater or Equal to (>=) 61 on the ETDRS Diabetic Retinopathy Severity Scale (DRSS) as Assessed by Fundus Photography (FP)(Baseline, Week 52)
  • Change From Baseline to Week 52 in Best Corrected Visual Acuity (BCVA) (Early Treatment Diabetic Retinopathy Study [ETDRS] Letter Score])(Baseline, Week 52)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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