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

Finnsusp

Status: Completed

Conditions: Adverse Reaction to Contact Lens Solution

Treatments: Device: Contact lens care solution

Study type: Interventional

Funder types: Industry

Identifiers

NCT01665612

FI-2012

Details and patient eligibility

About

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).

Enrollment: 40 patients

Sex: All

Ages: 18 to 60 years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

40 participants in 3 patient groups

MPDS1

Experimental group

Description:

Contact lens care solution

Treatment:

Device: Contact lens care solution

MPDS2

Active Comparator group

Description:

Contact lens care solution

Treatment:

Device: Contact lens care solution

MPDS3

Active Comparator group

Description:

Contact lens care solution

Treatment:

Device: Contact lens care solution