The Evaluation of the Clinical and Subjective Performance of Three Different Contact Lens Care Solutions With Silicon Hydrogel Lenses

Finnsusp Ltd.1 site in 1 country40 target enrollmentAugust 2012

ConditionsAdverse Reaction to Contact Lens Solution

Overview

Phase: N/A
Intervention: Not specified
Conditions: Adverse Reaction to Contact Lens Solution
Sponsor: Finnsusp Ltd.
Enrollment: 40
Locations: 1
Primary Endpoint: Clinical performance
Status: Completed
Last Updated: 11 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of the clinical investigation is to assess the clinical and subjective performance of three novel multipurpose disinfecting solutions (MPDS) in daily wear with two silicone hydrogel contact lenses (Lotrafilcon B and Comfilcon A).

Registry

clinicaltrials.gov

Start Date

August 2012

End Date

January 2015

Last Updated

11 years ago

Study Type

Interventional

Study Design

Crossover

Sex

All

Investigators

Sponsor

Finnsusp Ltd.

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•age above 18
•experienced contact lens user
•good health (self-reported)

Exclusion Criteria

•eye disease or eye operations
•pregnancy
•medication that can affect sight

Outcomes

Primary Outcomes

Clinical performance

Time Frame: 1 month

TBUT, conjunctival and limbal hyperemia, corneal vascularization, epithelial and stromal oedema, corneal infiltrates, endothelial regularity, corneal staining and papillar conjunctivitis