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

Optical Quality After Implantation of a Spherical or Aspherical Intraocular Lens in Hypermetropic Patients: A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01995630
Enrollment
62
Registered
2013-11-26
Start date
2013-11-30
Completion date
2016-06-26
Last updated
2017-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cataract, Depth of Focus, Intraocular Lenses, Spherical Aberrations

Brief summary

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.

Interventions

DEVICEAMO Tecnis ZA9003
DEVICEAMO Sensar AR40e

Sponsors

Medical University of Graz
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
40 Years to 80 Years
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frame
Distance-corrected intermediate visual acuity3 month postop

Secondary

MeasureTime frame
Uncorrected distance visual acuity3 month postop
Corrected distance visual acuity3 month postop
Uncorrected near visual acuity3 month postop
Corrected near visual acuity3 month postop
Distance-corrected near visual acuity3 month postop
Photopic contrast sensitivity3 month postop
Mesopic contrast sensitivity3 month postop
Spherical aberrations3 month postop
High order aberrations3 month postop
Pseudoaccomodation3 month postop

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026