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Non Contact Lens Wearers for Dry Eye Syndrome

N/A
Waitlist Available
Led By Lyndon Jones, PhD
Research Sponsored by Coopervision, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights

Study Summary

This study is being conducted to determine if scleral lenses coated with Hydra-PED improve comfort and dryness.

Eligible Conditions
  • Dry Eye Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
overall ocular comfort

Trial Design

2Treatment groups
Experimental Treatment
Group I: Non Contact Lens WearersExperimental Treatment1 Intervention
Each group will be a prospective, randomized, double masked, cross-over, 1-month per arm, daily wear study. Each participant will be active in the study for at least 2 months.
Group II: Habitual Soft Lens WearersExperimental Treatment1 Intervention
Each group will be a prospective, randomized, double masked, cross-over, 1-month per arm, daily wear study. Each participant will be active in the study for at least 2 months.

Find a Location

Who is running the clinical trial?

Coopervision, Inc.Lead Sponsor
155 Previous Clinical Trials
13,819 Total Patients Enrolled
Lyndon Jones, PhDPrincipal InvestigatorDirector, Centre for Ocular Research and Education
9 Previous Clinical Trials
442 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~6 spots leftby Apr 2025