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Clinical Analysis of Two Toric Intraocular Lenses

H

Hospital Hietzing

Status

Completed

Conditions

Cataract
IOL

Treatments

Device: intraocular lenses

Study type

Observational

Funder types

Other

Identifiers

NCT03371576
HHietzing

Details and patient eligibility

About

Purpose: Comparison of two torical intraocular lenses with differents haptic design in patients with cataract.

Methods: In this prospective, randomized clinical trial 120 eyes of 60 patients underwent phacoemulsification. In patient's eyes the Tecnis torical IOL (Abbott Medical Optics) or the AT Torbi torical 709 MB IOL (Zeiss Medical AG) were randomly implanted. Three months after surgery visual acuity, rotation stability and astigmatism correction were evaluated.

Enrollment

60 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age related cataract on both eyes
  • Corneal astigmatism 1,0- 4,0 D
  • Potential postoperative visus 1,0
  • No other ocular pathology as cataract
  • Age 18 - 80
  • Written informed consent to surgery and participation in the study

Exclusion criteria

  • Pregnancy, breastfeeding
  • Amblyopy, diabetic retinopathy, uveitis or other relevant ophthalmologic diseases
  • Optical media disturbances due to: corneal and vitreal opacity, PEX
  • Irregular astigmatism measured with corneal topography (Visante-omni), keratoconus
  • ≥ 10 degrees difference between the axis of keratometry measurement of the IOL Master and the simulated K reading of the corneal topograph (Visante-omni)
  • Trauma, ocular surgery performed within 6 months
  • Traumatic cataract
  • Potential postoperative visus under 1,0

Trial design

60 participants in 1 patient group

2 different torical intraocular lenses
Treatment:
Device: intraocular lenses

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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