MedTrace Logo

Evaluation of Two Toric Soft Contact Lenses After Two Weeks of Wear

NCT00584220 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 96

Last updated 2015-05-21

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to determine the relative performance of a new toric soft contact lens against a toric contact lens currently available in market, specifically with regards to the comfort and vision after two weeks of use.

Conditions

  • Astigmatism

Interventions

DEVICE

senofilcon A toric

contact lens

DEVICE

alphafilcon A toric

contact lens

Sponsors & Collaborators

  • Foresight Regulatory Strategies, Inc.

    collaborator INDUSTRY

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Jason Chin, O.D.

  • James Fujimoto, O.D.

  • Weslie Hamada, O.D. · Arthur T. Kobayashi, O.D., Inc.

  • Dennis Kuwuabara, O.D. · Eye Care Associates of Hawaii

  • Mark Nakano, O.D. · Mark E. Nakano Optometric Corp.

  • Ikuko Sugimoto, O.D. · Unaffilliated

  • Kevin Rosin, O.D. · Drs. Farkas, Kassalow, Resnick & Associates

  • Jennifer Kao, O.D.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2007-12-31
Completion
2007-12-31

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 NCT00584220 on ClinicalTrials.gov