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

NCT01665612 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2015-03-06

No results posted yet for this study

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).

Conditions

  • Adverse Reaction to Contact Lens Solution

Interventions

DEVICE

Contact lens care solution

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

Sponsors & Collaborators

  • Finnsusp Ltd.

    lead INDUSTRY

Principal Investigators

  • Riikka Järvinen, PhD · University of Turku, Finland; Finnsusp Ltd, Finland

  • Hanna Vaahtoranta-Lehtonen, Dr. Ophth. · Turku University Hospital

Study Design

Allocation
RANDOMIZED
Masking
TRIPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-08-31
Primary Completion
2015-01-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01665612 on ClinicalTrials.gov