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The Impact of Hypo-osmolar Drops on Contact Lens Comfort

NCT03050125 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2017-05-04

No results posted yet for this study

Summary

This pilot study will investigate the impact of sterile saline drops that are formulated at hypo-osmolar levels on CL comfort in comparison to an iso-osmolar drop, in a group of symptomatic CL wearers.

Conditions

  • Contact Lens Related Dry Eye

Interventions

DEVICE

Hypo-osmolar drop 1

180 mOsmol sterile saline drops used as a contact lens rewetting drop.

DEVICE

Hypo-osmolar drop 2

240 mOsmol sterile saline drops used as a contact lens rewetting drop.

DEVICE

Iso-osmolar drop

300 mOsmol sterile saline drops used as a contact lens rewetting drop.

Sponsors & Collaborators

  • CooperVision, Inc.

    collaborator INDUSTRY

  • Centre for Contact Lens Research

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-02-07
Primary Completion
2017-03-28
Completion
2017-03-28

Countries

  • Canada

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 NCT03050125 on ClinicalTrials.gov