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Visual Quality Following Aspheric Intraocular Lens (IOL) Implantation - a Comparative Clinical Study

NCT01544777 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2015-03-25

No results posted yet for this study

Summary

To evaluate visual acuity and quality of vision in participants undergoing cataract surgery with a Hoya model 751 intra-ocular lens and to compare the visual results to the common monofocal lens in use.

Conditions

  • Aphakia
  • Cataract

Interventions

DEVICE

Study IOL

Aspheric IOL for correction of aphakia

DEVICE

Hoya iSert 751

Model 751 in one eye, standard IOL in other eye

DEVICE

Negatively aspheric IOL

Negatively aspheric IOL in both eyes

Sponsors & Collaborators

  • Hoya Surgical Optics, Inc.

    lead INDUSTRY

Principal Investigators

  • Graham Barrett, MD · Sir Charles Gairdner Hospital, Nedlans WA

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
FACTORIAL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-02-29
Primary Completion
2012-08-31
Completion
2012-08-31

Countries

  • Australia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01544777 on ClinicalTrials.gov