RecruitingPhase 4NCT07510620

Single-Arm Study of a Treatment for Dry Eye in People Who Struggle to Wear Contact Lenses

Prospective, Single Arm Clinical Trial for the Treatment of Dry Eyes Signs and Symptoms in Patients With Limited Tolerability of Contact Lens Wear


Sponsor

Vision Innovation Centers of Pennsylvania, LLC d/b/a Eye Care Specialists

Enrollment

30 participants

Start Date

Dec 12, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 22 Years

Inclusion Criteria7

  • \>21 years of age
  • Contact lens wearer
  • Previous Dry Eye Treatment
  • Be on a stable dose of antihistamines/Birth Control Medication and Lifitegrast and cyclosporine.
  • Schrimers Anesthetized less than or equal to 10
  • CLDEQ-8 greater than or equal to 12
  • Corneal Staining NEI grading scale greater than or equal to 1

Exclusion Criteria9

  • Known allergy to Hyaluronic Acid
  • Current topical ophthalmic drops other than dry eye treatment
  • Uncontrolled Diabetes
  • Diabetic Retinopathy
  • Pregnancy or Lactating
  • Corneal Surgery (except Refractive)
  • Corneal Scars
  • Keratoconus
  • Ocular Herpetic Keratitis

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGLacrifill

Lacrifill is a cross-linked hyaluronic acid derivative that temporarily blocks tear drainage, allowing patients eyed to be bathed in their own natural tears.


Locations(1)

Eye Care Specialists

Kingston, Pennsylvania, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07510620


Related Trials