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OpenTrials
Completed

NCT Number: NCT00363623

Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses

The primary purpose of this study is to investigate the performance of contact lens maintenance systems when used with silicone hydrogel contact lenses during daily wear over a period of 1 month.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinical Vision Research Australia

Carlton, Victoria, 3053, Australia

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Is correctable to at least 20/40 distance visual acuity in each eye with spherical contact lenses.
  • Is an experienced soft contact lens wearer for at least 1 month.
  • Has no clinically significant anterior eye findings.
  • Has no other active ocular disease.

Exclusion criteria

  • Requires concurrent ocular medication.
  • Eye surgery or injury within 12 weeks prior to enrolment.
  • Has any systemic disease or ocular abnormality that might interfere with contact lens wear
  • Has any pre-existing ocular irritation that would preclude contact lens fitting.
  • PMMA lens wear previous 6 months.
  • EW or CW in previous 1 month.
  • Hydrogen peroxide users
  • Latex sensitivity

Treatment and study plan

silicone hydrogel contact lens

Device

Sponsors and collaborators

Lead sponsor

University of Melbourne

Other

Collaborators

  • CIBA VISION

Registry information

Important dates

Study start
2006
Study completion
2006
First posted
Aug 15, 2006
Registry last updated
Mar 21, 2008

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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