跳至主要内容
临床试验/NCT01872000
NCT01872000终止不适用

A Prospective Randomised Controlled Trial to Assess Improved Binocular Visual Function in Young Patients Undergoing Monocular Cataract Surgery With a Bifocal Intraocular Lens.

University of Oxford2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2013年4月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
12
试验地点
2
主要终点
Extent of binocular vision at near working distance following IOL implantation.

研究概览

简要总结

Following cataract surgery, an intraocular lens (IOL) is implanted in the eye. The majority of people develop an operable cataract when they are over the age of 50. Occasionally people under 50 years develop a cataract requiring an operation. The visual demands in this age group are very different due to both physiological and lifestyle factors. Traditionally IOLs are focussed for distance vision and additional spectacles are worn for near vision. Under the age of 45 years we have the ability to naturally change the focus of our eyes and do not require additional reading glasses. This is known as accommodation. By removing the cataractous lens and replacing it with an IOL with a fixed single focus, both eyes work together for distance vision but only the unoperated eye is able to change focus for different working distances. This study aims to establish whether a multifocal IOL implanted in one eye is able to complement the accommodation in the other eye so the 2 eyes work more effectively together. This may enhance depth perception and improve the quality of vision. Depth perception is important for more comfortable vision on the computer screen, when reading and for jobs that require good depth perception.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Participant is willing and able to give informed consent for participation in the study.
  • •Male or female, aged 18 -
  • •Cataract operation required in one eye only, either due to the presence of cataract affecting visual function, or in combination with surgery which is likely to cause visually significant cataract.
  • •Expected visual improvement in operable eye of at least 6/
  • •Fellow eye with a VA of at least 6/
  • •Astigmatism of 1.0D or less.
  • •Target of emmetropia in the operated eye.
  • •Intact posterior capsule with planned implantation into the capsular bag.
  • •IOL power required 10 - 30D.

排除标准

  • •Pre-existing amblyopia or squint.
  • •Significant diabetic retinopathy.
  • •Macular off retinal detachment with metamorphopsia or poor visual prognosis.
  • •Other macula or ophthalmic pathology affecting macula function resulting in poor visual prognosis.
  • •Pregnancy, lactating or planned pregnancy during the study period.

研究组 & 干预措施

Multifocal IOL

Experimental

Phacoemulsification and IOL inserted following cataract surgery

干预措施: Cataract surgery (Procedure)

Standard IOL

Active Comparator

Phacoemulsification and IOL inserted following cataract surgery

干预措施: Cataract surgery (Procedure)

结局指标

主要结局

Extent of binocular vision at near working distance following IOL implantation.

时间窗: 3-6 months

次要结局

  • Change in visual acuity and subjective visual comfort at distance, intermediate and near working distances following IOL implantation.(3-6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验