The Clinical and Subjective Performance of Three Different MPDS With Silicon Hydrogel Lenses

Finnsusp Ltd.40 enrolled

Overview

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).

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Masking

TRIPLE

Enrollment

Conditions

Adverse Reaction to Contact Lens Solution

Interventions

Contact lens care solutionDEVICE

Comparison of clinical and subjective performation of the contact lens care solutions used with two types of contact lenses

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

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

Locations (1)

Raision Näkökulma

Raisio, Finland

Outcomes

Primary Outcomes

Clinical performance

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

Time frame: 1 month

Secondary Outcomes

Subjective performance

E.g. Comfort

Time frame: 1 month

Data from ClinicalTrials.gov

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