MedTrace Logo

Clinical Evaluation of a 1-Piece Intraocular Lens

NCT01098812 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 269

Last updated 2025-02-04

Study results available
· View outcomes & findings →

Summary

The aims of this study are to:

* Demonstrate a reduction in postoperative cylinder compared to results from the control lens
* Demonstrate better uncorrected distance visual acuity compared to the control lens

Conditions

  • Cataract

Interventions

DEVICE

Tecnis ZCB00 IOL (control)

Tecnis 1-piece acrylic IOL

DEVICE

Toric Intraocular lens

Toric acrylic intraocular lens with various cylinder powers

Sponsors & Collaborators

  • Abbott Medical Optics

    lead INDUSTRY

Principal Investigators

  • Nicholas Tarantino, O.D. · Abbott Medical Optics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2011-10-31
Completion
2011-10-31

More Related Trials

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 NCT01098812 on ClinicalTrials.gov