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Changes in Invitro and ex Vivo Lens Metrology With Daily Wear Contact Lenses

NCT01100411 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2012-07-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate changes in contact lens geometry after lens wear

Conditions

  • Myopia

Interventions

DEVICE

Air Optix Aqua

Contact lens material: Lotrafilcon A

DEVICE

Biofinity

Contact lens material: Comfilcon A

DEVICE

Proclear

Contact lens material: Omafilcon A

DEVICE

Acuvue Oasys

Contact lens material: Senofilcon A

DEVICE

Acuvue 2

Contact lens material: Etafilcon A

DEVICE

Purevision

Contact lens material: Balafilcon A

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Principal Investigators

  • Alcon Call Center · Alcon Research

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2010-07-31
Completion
2010-07-31

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 NCT01100411 on ClinicalTrials.gov