Viewing Study NCT05505292


Ignite Creation Date: 2025-12-24 @ 3:35 PM
Ignite Modification Date: 2025-12-28 @ 10:37 AM
Study NCT ID: NCT05505292
Status: COMPLETED
Last Update Posted: 2025-01-14
First Post: 2022-08-16
Is Gene Therapy: True
Has Adverse Events: True

Brief Title: Lifitegrast 5% for the Treatment of Dry Eye In Habitual Soft Contact Lens Wearers
Sponsor: State University of New York College of Optometry
Organization:

Study Overview

Official Title: Lifitegrast 5% for the Treatment of Dry Eye In Habitual Soft Contact Lens Wearers
Status: COMPLETED
Status Verified Date: 2025-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a prospective, single site, randomized, double masked, comparator-controlled study designed to evaluate the efficacy of lifitegrast ophthalmic solution 5% in treating the symptoms of dry eye in soft contact lens wearers as compared to control. We hypothesize that there will be a significant improvement in dry eye symptoms in contact lens wearers using lifitegrast as compared to those being treated with control (lifitegrast vehicle).
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: