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OpenTrials
Completed

NCT Number: NCT01010555

In-vivo Wettability Grading and Assessment Study

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

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Key information

Conditions

Myopia Eye Diseases Refractive Errors

Age range

17 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Centre for Contact Lens Research: University of Waterloo

Waterloo, Ontario, N2L 3G1, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • is at least 17 years of age
  • has read and signed an information consent letter
  • is a current daily wear contact lens wearer
  • has acceptable fit with the study lenses
  • has had an ocular exam in the last two years
  • other protocol-defined inclusion criteria may apply

Exclusion criteria

  • has any ocular disease
  • has undergone corneal refractive surgery or is aphakic
  • has any systemic disease affecting ocular health
  • is pregnant or lactating
  • other protocol-defined exclusion criteria may apply

Treatment and study plan

lotrafilcon B

Device

Commercially marketed, silicone hydrogel, spherical contact lens

Other names: Air Optix

balafilcon A

Device

Commercially marketed, silicone hydrogel, spherical contact lens

Other names: PureVision

Senofilcon A

Device

Commercially marketed, silicone hydrogel, spherical contact lens

Other names: Acuvue OASYS

enfilcon A

Device

Commercially marketed, silicone hydrogel, spherical contact lens

Other names: Avaira

Primary outcomes

  1. On-eye Wettability

    Time frame: 4 weeks of wear

    On-eye wettability, as assessed at the 4-week visit by a masked observer from a video taken of the eye 5 minutes after lens insertion. On-eye wettability was recorded on a 5-point scale, with 0=excellent and 4=very poor.

Sponsors and collaborators

Lead sponsor

CIBA VISION

Industry

Collaborators

  • University of Waterloo

Registry information

Acronym: CIAN

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Nov 10, 2009
Registry last updated
Jul 10, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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