Silicone Hydrogel Contact Lenses on Low Astigmatism in Japan

NCT00639353 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2014-10-29

No results posted yet for this study

Summary

This study seeks to evaluate the clinical performance of a recently released contact lens designed to correct astigmatism to an established contact lens that has historically been used in these patients.

Conditions

  • Refractive Error
  • Myopia
  • Astigmatism

Interventions

DEVICE

senofilcon A toric soft contact lens

contact lens

DEVICE

senofilcon A sphere soft contact lens

contact lens

Sponsors & Collaborators

  • Johnson & Johnson

    collaborator INDUSTRY
  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

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
2008-02-29
Primary Completion
2008-06-30

Countries

  • Japan

Study Locations

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Entities

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 NCT00639353 on ClinicalTrials.gov