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Optical Quality After Implantation of a Spherical or Aspherical Intraocular Lens in Hypermetropic Patients

M

Medical University of Graz

Status

Completed

Conditions

Cataract
Spherical Aberrations
Depth of Focus
Intraocular Lenses

Treatments

Device: AMO Sensar AR40e
Device: AMO Tecnis ZA9003

Study type

Interventional

Funder types

Other

Identifiers

NCT01995630
SIOLvsAIOL

Details and patient eligibility

About

The purpose of this study is to evaluate differences in the depth of focus after implantation of a spherical or aspheric IOL in hypermetropic and emmetropic patients. After implantation of a spherical IOL hypermetropic patients may achieve a better depth of focus compared to emmetropic patients due to a larger amount of spherical aberrations.

Enrollment

62 patients

Sex

All

Ages

40 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cataract
  • Dioptric power of IOL >22.0 D in hypermetropic patients and 18.0-22.0 D in emmetropic patients, respectively

Exclusion criteria

  • Uveitis, pathology of the retina or the optic nerve
  • Corneal scarring or irregularities
  • Astigmatism >1.5 D
  • Amblyopia
  • Perioperative complications
  • Postoperative refractive error >2.0 D of spherical equivalent
  • Postoperative DCVA <0.8 (ETDRS)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

62 participants in 4 patient groups

Hypermetropic, spherical IOL
Experimental group
Description:
AMO Sensar AR40e
Treatment:
Device: AMO Sensar AR40e
Hypermetropic, aspheric IOL
Experimental group
Description:
AMO Tecnis ZA9003
Treatment:
Device: AMO Tecnis ZA9003
Emmetropic, spherical IOL
Active Comparator group
Description:
AMO Sensar AR40e
Treatment:
Device: AMO Sensar AR40e
Emmetropic, aspheric IOL
Active Comparator group
Description:
AMO Tecnis ZA9003
Treatment:
Device: AMO Tecnis ZA9003

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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