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Subjective and Conjunctival Response to Edge Design of Different Silicone Hydrogels

NCT00940459 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-11-16

No results posted yet for this study

Summary

The purpose of this study was to evaluate the effect of different contact lens edge designs on the circumlimbal conjunctiva.

Conditions

  • Contact Lenses

Interventions

DEVICE

Senofilcon A contact lens (Acuvue Oasys)

Silicone hydrogel contact lens CE-marked for the intended usage.

DEVICE

Comfilcon A contact lens (Biofinity)

Silicone hydrogel contact lens CE-marked for the intended usage.

DEVICE

Lotrafilcon B contact lens (Air Optix)

Silicone hydrogel contact lens CE-marked for the intended usage.

DEVICE

Balafilcon A contact lens (PureVision)

Silicone hydrogel contact lens CE-marked for the intended usage.

DEVICE

Etafilcon A contact lens (Acuvue 2)

Hydrogel contact lens CE-marked for the intended usage.

DEVICE

Contact lens care system (EasySept)

Contact lens care system CE-marked for the intended usage.

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2009-09-30
Completion
2009-09-30

Countries

  • United Kingdom

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 NCT00940459 on ClinicalTrials.gov