MedTrace Logo

In-vivo Wettability Grading and Assessment Study

NCT01010555 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2012-07-10

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to investigate the front surface wettability of soft contact lenses while on eye.

Conditions

  • Myopia

Interventions

DEVICE

lotrafilcon B

Commercially marketed, silicone hydrogel, spherical contact lens

DEVICE

balafilcon A

Commercially marketed, silicone hydrogel, spherical contact lens

DEVICE

senofilcon A

Commercially marketed, silicone hydrogel, spherical contact lens

DEVICE

enfilcon A

Commercially marketed, silicone hydrogel, spherical contact lens

Sponsors & Collaborators

  • University of Waterloo

    collaborator OTHER

  • CIBA VISION

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-10-31
Primary Completion
2010-04-30
Completion
2010-04-30

Countries

  • Canada

Study Locations

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 NCT01010555 on ClinicalTrials.gov