Your session is about to expire
← Back to Search
Artificial Tears
Systane® Hydration Eye Drops for Dry Eye Syndrome
N/A
Recruiting
Research Sponsored by Alcon Research
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up visit 3 (day 30)
Awards & highlights
Study Summary
This trial will assess the performance and safety of eye drops for dry eye relief in different groups of people. Results will be presented by group.
Who is the study for?
This trial is for individuals with mild to moderate dry eye symptoms, including those who wear contact lenses and experience discomfort due to dryness. Participants must understand and sign a consent form. People who've had recent ocular surgery or injury are excluded.Check my eligibility
What is being tested?
The study compares the performance and safety of two eye drop solutions: Systane Hydration PF (preservative-free) for general dry eye, and both Systane Hydration PF & Preserved in contact lens wearers with dryness.See study design
What are the potential side effects?
Potential side effects may include temporary visual disturbances, stinging or burning sensation in the eyes, excessive tearing, eyelid irritation or redness, and possible allergic reactions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ visit 3 (day 30)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~visit 3 (day 30)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mean overall IDEEL-Symptom Bother(SB) score - Group 1
Resultant overall CLDEQ-8 score - Group 2 and Group 3
Trial Design
2Treatment groups
Experimental Treatment
Group I: Systane Hydration PreservedExperimental Treatment1 Intervention
1-2 drops in each eye four times a day for 30 days
Group II: Systane Hydration Preservative Free (PF)Experimental Treatment1 Intervention
1-2 drops in each eye four times a day for 30 days
Find a Location
Who is running the clinical trial?
Alcon ResearchLead Sponsor
704 Previous Clinical Trials
124,376 Total Patients Enrolled
Clinical Lead, Vision CareStudy DirectorAlcon Research, LLC
2 Previous Clinical Trials
135 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I experience dry eyes due to my contact lenses.I have had an eye injury in the last 3 months.I have not had eye surgery in the last 6 months and do not plan any during the study.I have mild to moderate dry eye condition.
Research Study Groups:
This trial has the following groups:- Group 1: Systane Hydration Preservative Free (PF)
- Group 2: Systane Hydration Preserved
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are any new participants being sought for this research project?
"Contrary to what is reported on clinicaltrials.gov, this trial is not seeking out any more participants. After the initial posting of July 1st 2023 and an update on June 27th 2023, it has become inactive; however, there are 90 other trials actively recruiting patients at present."
Answered by AI
Share this study with friends
Copy Link
Messenger