Actively Recruiting
Single-Arm Study of a Treatment for Dry Eye in People Who Struggle to Wear Contact Lenses
Led by Vision Innovation Centers of Pennsylvania, LLC d/b/a Eye Care Specialists · Updated on 2026-04-03
30
Participants Needed
1
Research Sites
33 weeks
Total Duration
On this page
Sponsors
V
Vision Innovation Centers of Pennsylvania, LLC d/b/a Eye Care Specialists
Lead Sponsor
N
Nordic Pharma, USA
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research study is to see if using Lacrifill is safe, easy to use, and helpful for people who wear contact lenses but can't wear them comfortably for long. Specifically, the study aims to determine whether regular use of Lacrifill over a 2-3 month period can help people wear their contacts longer without discomfort and reduce signs and symptoms of dry eye.
CONDITIONS
Official Title
Single-Arm Study of a Treatment for Dry Eye in People Who Struggle to Wear Contact Lenses
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Over 21 years of age
- Current contact lens wearer
- Previous treatment for dry eye
- On a stable dose of antihistamines, birth control medication, Lifitegrast, or cyclosporine
- Schirmer's test (anesthetized) result less than or equal to 10
- Contact Lens Dry Eye Questionnaire (CLDEQ-8) score greater than or equal to 12
- Corneal staining score on NEI grading scale greater than or equal to 1
You will not qualify if you...
- Known allergy to Hyaluronic Acid
- Using topical eye drops other than dry eye treatments
- Uncontrolled diabetes
- Diabetic retinopathy
- Pregnant or breastfeeding
- History of corneal surgery except refractive surgery
- Presence of corneal scars
- Diagnosis of keratoconus
- History of ocular herpetic keratitis
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Eye Care Specialists
Kingston, Pennsylvania, United States, 18704
Actively Recruiting
Research Team
P
Patti Myers, COT
CONTACT
C
Cheryl Bayley
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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