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临床试验/NCT02157350
NCT02157350已完成3 期

A Prospective Study to Identify Predictive Factors for Progression and Regression of Proliferative Diabetic Retinopathy in Patients Receiving Standard Panretinal Laser Photocoagulation.

Odense University Hospital2 个研究点 分布在 1 个国家目标入组 65 人开始时间: 2014年8月最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
65
试验地点
2
主要终点
Proliferative diabetic retinopathy progression/regression.

研究概览

简要总结

The purpose of this study is to determine the threshold level of proliferative diabetic retinopathy progression and regression after standard panretinal photocoagulation. Predictors of progression and regression will be identified which will include retinal vessel geometry (caliber, fractals and tortuosity), retinal vessel oxygen saturation and retinal areas of non-perfusion.

详细描述

IMPETUS 2018 - DETECT is a six-month prospective study involving 90 treatment-naïve diabetes patients with proliferative diabetic retinopathy (PDR) referred for panretinal laser photocoagulation (PRP) treatment to the Department of Ophthalmology, Odense University Hospital between July 1st 2014 and June 30th 2015.

Project information will be given prior to the study to the ophthalmological departments of and to all private practicing ophthalmologists in the Region of Southern Denmark. Patients will at baseline have a standard examination that will include wide-field fundus photography, wide-field fluorescein angiography and spectral domain optical coherence tomography (SD-OCT) in order to confirm the diagnosis of PDR. If they meet the criteria of inclusion and not those of exclusion, they will be informed of the study verbally and writing and offered the chance to participate. Prior to the first session of PRP patients enrolled in the study will receive the rest of the baseline examinations including retinal oximetry. Standard PRP treatment will be given in two sessions by a trained doctor.

Patients will be re-examined at month 3 and 6 and progression/regression of PDR will be evaluated by measuring the amount of fluorescein leakage by wide-field fluorescein angiography at 1, 5 and 10 minutes. For patients with regression, supplementary PRP will be offered. After the final examination at month 6, patients will be referred back to their primary ophthalmologist.

A study nurse and a photographer will be assigned to the project. All examinations will be standardized and the study crew will be fully certified. Data will be analyzed with respect to the endpoint of the study (Stata 13, StataCorp, College Station, Texas) and also used to create the algorithm to be used for individualized treatment in IMPETUS 2018 - TREAT.

In the Region of Southern Denmark it is estimated that 200 treatment naïve patients with PDR will be referred for treatment annually. With an estimated participation rate of 50% and a subsequent dropout rate of 10%, IMPETUS 2018 - DETECT will include 90 patients. A traditional power calculation is not feasibly due to the design of the study with multiple outcomes studies.

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 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diabetes mellitus
  • Proliferative diabetic retinopathy of one or both eyes

排除标准

  • Diabetic macular edema on current eye
  • Earlier PRP treatment on current eye
  • Cataract demanding treatment on current eye
  • Pregnancy

研究组 & 干预措施

Panretinal Laser Photocoagulation

Experimental

See interventional description.

干预措施: Panretinal laser photocoagulation (Procedure)

结局指标

主要结局

Proliferative diabetic retinopathy progression/regression.

时间窗: Change from baseline in proliferative diabetic retinopathy at 6 months

Progression/regression of proliferative diabetic retinopathy will be evaluated by measuring the amount of fluorescein leakage by wide-field fluorescein angiography at 1, 5 and 10 minutes. These measurements will be performed at baseline, and during followup after panretinal photocoagulation (3 months and 6 months).

次要结局

  • Retinal vessel geometry (caliber, fractals and tortuosity)(Measurements assessed at baseline and 3 and 6 months after panretinal laser photocoagulation.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Thomas Lee Torp

MD

Odense University Hospital

研究点 (2)

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