Comparison of Contact Lens Maintenance Systems for Silicone Hydrogel Lenses

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00363623

Enrollment

Registered

2006-08-15

Start date

2006-08-31

Completion date

2006-12-31

Last updated

2008-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hyperopia, Myopia

Brief summary

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.

Interventions

DEVICESilicone hydrogel contact lens

Study design

Allocation

RANDOMIZED

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

SINGLE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

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

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026