此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

The Influence of Silicone Oil on Nerve Fiber Layer Thickness After Pars Plana Vitrectomy

2012年3月22日 更新者:Mia Zoric Geber、University Hospital "Sestre Milosrdnice"
The aim of the study is to evaluate the influence of silicone oil on thickness of the retinal nerve fiber layer by using optical coherence tomography (OCT) in patients following pars plana vitrectomy.

研究概览

详细说明

The aim of the study is to evaluate the influence of silicone oil on thickness of the retinal nerve fiber layer by using optical coherence tomography (OCT) in patients following pars plana vitrectomy.

The study will include 60 patients with a temporary silicone oil tamponade who will be surgically treated with pars plana vitrectomy for rhegmatogenous retinal detachment and proliferative vitreoretinopathy. All subjects will be subdued to complete ophthalmologic examinations, measurements of the retinal nerve fiber layer thickness by an OCT examination, tests of the visual field with the use of an Octopus computed perimeter (automated static perimetry) and FDT-perimetry - both prior to the surgery, and on control visits for check-up during the postoperative period.

All results provided by postoperative examinations will be compared with one another.

The study is expected to provide data on the effect of the silicone oil on thickness of the retinal nerve fiber layer. It is also planned to show possibilities and advantages of OCT as a method of choice in the follow-up of patients with intraocular silicone oil tamponade.

研究类型

观察性的

注册 (实际的)

60

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Zagreb、克罗地亚、10000
        • University Department of Ophthalmology, University Hospital "Sestre milosrdnice", Vinogradska 29

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 80年 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

取样方法

概率样本

研究人群

tertiary care clinic

描述

Inclusion Criteria:

- patients with rhegmatogenous retinal detachment

Exclusion Criteria:

  • preexistent glaucoma
  • previous retinal surgery
  • placement of scleral buckle during surgery
  • patients with more than 1/2 of emulsified silicone oil in anterior chamber postoperatively
  • patients who develop silicone oil keratopathy postoperatively
  • patients who develop silicone oil cataract which blocks visualization of posterior segment

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 观测模型:病例对照
  • 时间观点:预期

队列和干预

团体/队列
干预/治疗
NO IOP
Patients without raised IOP

Optical coherence tomography will be performed in all study patients following pars plans vitrectomy and silicone oil tamponade. A fellow eye of each patient will serve as a control. Each patient enrolled in a study will receive 4 measurements:

  1. On 7th postoperative day
  2. On 30th postoperative day
  3. On 90th postoperative day
  4. On 180th postoperative day
其他名称:
  • Cirrus HD OCT ( Carl Zeiss Meditec, Dublin, CA )
RAISED IOP
Patients with raised IOP

Optical coherence tomography will be performed in all study patients following pars plans vitrectomy and silicone oil tamponade. A fellow eye of each patient will serve as a control. Each patient enrolled in a study will receive 4 measurements:

  1. On 7th postoperative day
  2. On 30th postoperative day
  3. On 90th postoperative day
  4. On 180th postoperative day
其他名称:
  • Cirrus HD OCT ( Carl Zeiss Meditec, Dublin, CA )

In patients with raised intraocular pressure following medications will be employed in order to control the intraocular pressure:

Cosopt (dorzolamide hydrochloride-timolol maleate ophthalmic solution; b.i.d.) Ganfort (Bimatoprost, timolol maleate ophthalmic solution; once daily) Alphagan (Brimonidine ophthalmic solution; b.i.d.) In patients with intraocular pressure less than 27 mmHg Alphagan will be prescribed. In patients with intraocular pressure greater than 27 mmHg either Cosopt, or Ganfort will be prescribed under the discretion of treating physician. If intraocular pressure in patients treated with either Cosopt or Ganfort does not drop under 21 mmHg, Alphagan will be added.

其他名称:
  • 1. Cosopt
  • 2. Ganfort
  • 3. Alphagan

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Evidence of Retinal Nerve Fibre Layer Thickness Change Measured by Optical Coherence Tomography
大体时间:6 months
Retinal nerve fiber layer thickness change measured by optical coherence tomography might be an additional parameter that could provide new insights into clinical decision making in patients with silicone oil tamponade.
6 months

次要结果测量

结果测量
措施说明
大体时间
Retinal Nerve Fiber Layer Thickness Change in Patients With Raised Intraocular Pressure Secondary to Silicone Oil Endotamponade
大体时间:6 months
To assess whether retinal nerve fiber layer thickness changes in patients with raised intraocular pressure secondary to silicone oil endotamponade.
6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Mia Zoric Geber, MD、University department of Ophthalmology, University Hospital "Sestre milosrdnice"

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2010年4月1日

初级完成 (实际的)

2011年11月1日

研究完成 (实际的)

2011年12月1日

研究注册日期

首次提交

2010年12月6日

首先提交符合 QC 标准的

2010年12月6日

首次发布 (估计)

2010年12月7日

研究记录更新

最后更新发布 (估计)

2012年3月23日

上次提交的符合 QC 标准的更新

2012年3月22日

最后验证

2012年3月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

孔源性视网膜脱离的临床试验

Optical coherence tomography的临床试验

3
订阅