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OpenTrials
Completed

NCT Number: NCT00768885

Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs.

To evaluate the wearing satisfaction of a new design of the PureVision soft contact lenses.

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Key information

Conditions

Myopia Eye Diseases Refractive Errors

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kodama Eye Clinic

Kyoto, 6100121, Japan

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Subject is myopic
  • Subjects who wear soft contact lenses that are exchanged at least biweekly at the time consent is obtained.

Exclusion criteria

  • Systemic disease affecting ocular health
  • Using pharmaceuticals that may affect the function of the eyes or lenses.
  • Subject possessing corneal infiltrate or corneal ulcers.

Treatment and study plan

PureVision 1

Device

Currently marketed PureVision soft contact lens.

PureVision 2

Device

Alternate design soft contact lens.

Primary outcomes

  1. Patient satisfaction

    Time frame: 4 weeks

Sponsors and collaborators

Lead sponsor

Bausch & Lomb Incorporated

Industry

Registry information

Official study title

Comparative Study of the Wearing Satisfaction of Two Soft Contact Lens Designs

Important dates

Study start
2008
Primary completion
2008
Study completion
2009
First posted
Oct 8, 2008
Registry last updated
Mar 18, 2013

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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