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Clinical Trials in the USA / NCT07629557
Recruiting Phase 4

Evaluate the Safety and Feasibility of Same-Day Bilateral Epithelium-On Corneal Cross-Linking for Keratoconus

NCT07629557 · tracked via the Priya Life Science USA tracker
Sponsor
Glaukos Corporation
Phase
Phase 4
Started
2026-05-11
Last updated
2026-06-05

Condition(s) studied

Keratoconus

Investigational drug(s) / intervention(s)

Riboflavin Ophthalmic SolutionsUV-A Irradiation System

Riboflavin Ophthalmic Solutions: Riboflavin Ophthalmic Solutions

UV-A Irradiation System: O2n UV-A Irradiation System

Study summary

Clinical trial to evaluate the safety and feasibility of corneal cross-linking in both eyes on the same day in subjects with keratoconus.

Eligibility

Sex
ALL
Min age
13 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Provide written informed consent * Willing and able to comply with study instructions and follow-up visits * Diagnosis of keratoconus in each eye Exclusion Criteria: * Known allergy or sensitivity to study medications * History of corneal disease * Prior corneal cross-linking in either eye * Pregnant, nursing, or planning pregnancy during the study period * Participated in other investigational drug or device trial within 30 days of the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Glaukos Investigative Site Westerville Ohio Recruiting

More Glaukos Corporation trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07629557 on ClinicalTrials.gov ↗ ← All trials in the USA