MedPath

Efficacy Study of a New Eyedrop on Silicone Hydrogel Contact Lens Wearers With Dry Eye Complaints

Phase 4
Completed
Conditions
Contact Lens Related Dry Eye Syndrome
Registration Number
NCT01543061
Lead Sponsor
Optometric Technology Group Ltd
Brief Summary

The objectives of the investigation will be to assess the effect of the repeated usage of a new eye drop on the tear film characteristics of silicone hydrogel contact lens wearers with contact lens related comfort problems and to quantify any potential benefit.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
35
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Primary Outcome Measures
NameTimeMethod
Tear Break up Time30 days
Secondary Outcome Measures
NameTimeMethod
Comfort, vision and ocular symptoms questionnaire30 days
Conjunctival staining measurement30 days
Ocular Surface Disease Index questionnaire30 days
Tear film evaporation rate30 days
Post wear contact lens deposition and lipid uptake assessment30 days

Trial Locations

Locations (1)

OTG Research & Consultancy

🇬🇧

London, United Kingdom

OTG Research & Consultancy
🇬🇧London, United Kingdom

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.