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临床试验/NCT03152500
NCT03152500已完成不适用

A Randomised, Subject-masked Evaluation of Stability After Implantation of Two Different Lens Models: FEMTIS-study

Maastricht University Medical Center1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2017年1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
已完成
入组人数
40
试验地点
1
主要终点
Decentration:To compare the amount of decentration between FEMTIS IOL versus a standard monofocal IOL (Acrysof monofocal IOL) using retro-illumination slitlamp photographs

研究概览

简要总结

In this study the investigators will investigate the stability of lens position and the visual outcome after implantation of the new FEMTIS-IOL using FLACS capsulotomy compared to conventional placement of the IOL in the capsular bag. So far, there are no published studies using the FEMTIS-IOL. Therefore, the investigators will perform this randomized control trial.

详细描述

Cataract is a clouding of the crystalline lens which causes vision loss and blindness if untreated. Cataract surgery is the most frequently performed surgical intervention in medicine with an incidence of 880 surgeries per 100.000 population in 2010 amounting to a total number of over 160.000 surgeries per year in the Netherlands.1,3 The number of individuals with cataracts is predicted to reach 30 million by the year 2020.2 Due to aging of the general population this number of cataracts will only grow in the future.

For the last decade conventional phacoemulsification cataract surgery (CPCS) is the dominant form of cataract surgery in developed countries, accounting for over 90 percent of these procedures.4 The basic phacoemulsification procedure has remained largely unchanged over the past 20 years, including a series of steps: creating corneal incision, capsulorhexis and lensfragmentation.4 Although highly successful, each of the steps mentioned above are created manually which affects the safety and effectiveness of the procedure.

Since the first human eye was treated by femtosecond laser cataract surgery in 2008, the femtosecond-laser assisted cataract surgery (FLACS) became an innovative growing new technology in the world of cataract surgery.4-7 Femtosecond-lasers are capable of performing some of the most delicate and essential key steps during cataract surgery: capsulotomy, lens fragmentation, and corneal incisions. 'Automating' these steps and performing them with increased precision could lead to an improved quality of capsulotomy, easier lens fragmentation, and more precisely positioned corneal incisions, which in turn, lead to improved visual and refractive outcomes, a decrease in intra- and postoperative complication rates, and increased quality of life.

In order to remove the crystallized human lens, a circular opening in the capsular lens bag, capsulotomy, needs to be created. After removing the lens an intraocular lens (IOL) can be inserted in the empty capsule bag. However, one of the factors affecting postoperative achieved visual acuity and refraction, is the behaviour of this IOL in the capsular bag. Preoperative measurements need to be obtained in order to calculate the required IOL. One of the challenges of these IOL calculations is determining exactly where in the eye the IOL will end up, the effective lens position (ELP). The position of the IOL is crucial for the IOL's general performance because it influences the postoperative IOL tilt, decentration, and posterior capsule opacification (PCO). Considering the anatomical variety between patients, the predictability of an individual's ELP remains an educated guess.

The ELP, and therefore the amount of IOL tilt, decentration and PCO, of an IOL is mainly influenced by the interaction between the IOL and the lens capsule, especially during the time of capsule shrinkage. Theoretically, the positive optical effect of an IOL is lost when there is more than 7 degrees of tilt or more than 0.4 mm of decentration.8 Furthermore, studies have shown the effect of axial displacement of an IOL on refractive error. There is approximately 1.25 D change per millimetre of the IOL's longitudinal displacement.9 This reflects the importance of a stable and predictable ELP.

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
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Minimum 40 years of age
  • •Cataracta Senilis
  • •Expected postoperative astigmatism ≤ 0.75 D (combination with FLACS AK is tolerated up to 1.25 D preoperative astigmatism)
  • •IOL power calculation between +10.00 D and 27.00 D
  • •Expected postoperative best-corrected visual acuity of logMAR +0.3 or better
  • •If eligible, availability to undergo second eye surgery within 2 weeks of the first eye surgery
  • •Willing and able to comply with scheduled visits and other study procedures
  • •Signed informed consent.

排除标准

  • •Traumatic cataract
  • •Previous corneal surgery and/or reshaping
  • •Clinically significant corneal endothelial dystrophy (e.g., Fuchs' dystrophy)
  • •Irregular astigmatism
  • •History of corneal disease (e.g., herpes simplex, herpes zoster keratitis, etc.)
  • •Extensive age related macular degeneration (atrophic or exudative age-related macular degeneration or numerous soft drusen)
  • •Extensive visual field loss (e.g., glaucoma, history of cerebral vascular accidents, etc.)
  • •Extensive diabetic macular disease
  • •Amblyopia, strabismus
  • •Keratoconus
  • •Pseudoexfoliation syndrome or other capsule or zonular abnormalities that could affect postoperative centration or tilt of the IOL
  • •Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils, or pupils that do not dilate at least 3.5 mm under mesopic/scotopic conditions)
  • •Cognitive, cerebral or concentration disorders (e.g. dementia, Parkinson, etc.)
  • •Suturing of incision required at time of surgery
  • •Complications during surgery of the first eye.

研究组 & 干预措施

FEMTIS IOL

Experimental

The FEMTIS-IOL has a special haptic system that allows the lens to clamp into the capsulorrhexis.

干预措施: FEMTIS 313G IOL (Device)

Acrysof IOL

Active Comparator

The Acrysof IOL has a flexible haptic design that keeps the IOL stable and centered in the capsular bag

干预措施: Acrysof SN60WF IOL (Device)

结局指标

主要结局

Decentration:To compare the amount of decentration between FEMTIS IOL versus a standard monofocal IOL (Acrysof monofocal IOL) using retro-illumination slitlamp photographs

时间窗: 13 weeks/3months

To compare the amount of decentration between FEMTIS IOL versus a standard monofocal IOL (Acrysof monofocal IOL) using retro-illumination slitlamp photographs

次要结局

  • Rotation stability(13 weeks/3months)
  • Visual outcomes(13 weeks/3months)
  • Tilt: To compare the amount of tilt between both IOls using Scheimpflug images(13 weeks/3months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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