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OpenTrials
Completed

NCT Number: NCT00441233

Clinical Performance of Extended Wear Silicone Hydrogel Lenses

The primary purpose of this study is to investigate the clinical performance of a new silicone hydrogel contact lens over a period of 6 months of extended wear.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinical Vision Research Australia

Melbourne, Victoria, 3053, Australia

Who can participate

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

Inclusion criteria

  • Is correctable to at least 6/9 distance visual acuity in each eye with spherical contact lenses.
  • Is a current daily wear soft contact lens wearer.
  • Has no clinically significant anterior eye findings.
  • Has no other active ocular disease.

Exclusion criteria

  • Has any systemic disease that might interfere with contact lens wear
  • Is using any systemic or topical medications that will affect ocular health.
  • Has any pre-existing ocular irritation that would preclude contact lens fitting.
  • Has any ocular pathology or severe insufficiency of lacrimal secretion (dry eyes) that would affect the wearing of contact lenses.
  • Has undergone corneal refractive surgery.
  • Is pregnant, lactating or planning a pregnancy.

Treatment and study plan

silicone hydrogel contact lens

Device

Sponsors and collaborators

Lead sponsor

University of Melbourne

Other

Collaborators

  • Clinical Vision Research Australia
  • Menicon Co., Ltd.

Registry information

Important dates

Study start
2007
Primary completion
2007
Study completion
2007
First posted
Feb 28, 2007
Registry last updated
Jan 9, 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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