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Clinical Trials/NCT03538964
NCT03538964
Unknown
Not Applicable

Assessing the Astigmatism Reducing Effect With Toric IOLs in Eyeswith Low Astigmatism

Prim. Prof. Dr. Oliver Findl, MBA1 site in 1 country25 target enrollmentMay 2, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
Prim. Prof. Dr. Oliver Findl, MBA
Enrollment
25
Locations
1
Primary Endpoint
Subjective refraction to detect remaining astigmatism (in Diopters) between both groups
Last Updated
6 years ago

Overview

Brief Summary

Comparison of the astigmatism reducing effect of a toric IOL with a non toric IOL in eyes with low corneal astigmatism.

Detailed Description

With increasing demands of patients concerning refractive outcome after cataract surgery, toric intraocular lenses (IOLs) that correct corneal astigmatism have been introduced more widely to cataract surgery. Originally, toric IOLs were used mainly for patients with high degrees of astigmatism. Since a couple of years, toric IOLs are available from numerous manufacturers to correct moderate amounts of astigmatism which are much more prevalent with about 8% having a corneal astigmatism of 2.0D or more in the cataract population. 5Using toric IOLs for these eyes results in less spectacle dependence of patients due to the astigmatic correction. Other astigmatism reducing techniques, such as peripheral corneal relaxing incisions and opposite clear corneal incisions were shown to be less predictable. Although the use of toric IOLs became the gold standard to correct corneal astigmatism during cataract surgery , there is still uncertainty, if low astigmatism should be corrected. Visser et al. showed that moderate astigmatism of than 1.5D should be corrected for monofocal IOLs and Hayashi showed that remaining astigmatism of 1.0D already decreases visual quality in eyes with multifocal IOLs. Although correction of low corneal astigmatism appears to be beneficial, some hurdles have to be taken into account. In eyes with low corneal astigmatism the accuracy of measuring the astigmatism meridian is relatively low. Furthermore, different corneal measurement techniques are not always comparable and it is difficult to know, which device shows the correct amount of astigmatism. Additionally, the correction of the spherical equivalent is of high importance, as a refractive surprise will also attenuate the astigmatism reducing effect of the toric IOL. Aim of this study is to assess, if toric IOLs are useful in patients with low amounts of corneal astigmatism and to quantify the sources of error in toric IOL power calculation.

Registry
clinicaltrials.gov
Start Date
May 2, 2018
End Date
August 1, 2020
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Prim. Prof. Dr. Oliver Findl, MBA
Responsible Party
Sponsor Investigator
Principal Investigator

Prim. Prof. Dr. Oliver Findl, MBA

Principal Investigator

Vienna Institute for Research in Ocular Surgery

Eligibility Criteria

Inclusion Criteria

  • Age 21 and older
  • Regular corneal astigmatism 0.5D up to 1.5 D and difference between eyes not more than 0.75D
  • written informed consent prior to surgery

Exclusion Criteria

  • relevant other ophthalmic diseases such as: pseudoexfoliation, glaucoma, traumatic cataract corneal scars, and other co-morbidity that could affect capsule bag stability ( e.g. Marfan syndrome)
  • Irregular corneal astigmatism on corneal topography
  • In case of pregnancy (pregnancy test will be taken preoperatively in women of reproductive age)

Outcomes

Primary Outcomes

Subjective refraction to detect remaining astigmatism (in Diopters) between both groups

Time Frame: 12 months

Secondary Outcomes

  • Wavefront analysis of high order aberrations (root mean square, in microns)(12 months)
  • Purkinjemeter measurement of Tilt (in degrees) and Decentration (in degrees) of the intraocular lens(12 months)
  • Biometrical measurement of axial length (in mm), anterior chamber depth (in mm), corneal astigmatism (radii and axial degrees)(12 months)
  • Questionnaire to asses patients subjective satisfaction with visual outcome(12 months)

Study Sites (1)

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