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RECRUITING
NCT05314738
PHASE1/PHASE2

Safety and Efficacy of Corneal Cross-linking in Subjects With Keratoconus

Sponsor: Glaukos Corporation

View on ClinicalTrials.gov

Summary

Clinical Trial to Evaluate the Safety and Efficacy of Corneal Cross-linking in Subjects with Keratoconus.

Official title: A Dose Ranging, Multicenter, Sham-Controlled Study to Evaluate the Safety and Efficacy of Corneal Cross-linking in Subjects With Keratoconus

Key Details

Gender

All

Age Range

18 Years - 55 Years

Study Type

INTERVENTIONAL

Enrollment

150

Start Date

2022-03-08

Completion Date

2026-02

Last Updated

2024-07-08

Healthy Volunteers

No

Interventions

COMBINATION_PRODUCT

NXL Energy 1

Riboflavin drops + NXL System to Total Energy Level 1

COMBINATION_PRODUCT

NXL Energy 2

Riboflavin drops + NXL System to Total Energy Level 2

COMBINATION_PRODUCT

NXL Energy 3

Riboflavin drops + NXL System to Total Energy Level 3

COMBINATION_PRODUCT

Sham Treatment

Sham Drops and No exposure to NXL system

Locations (3)

Glaukos Investigative Site

Dothan, Alabama, United States

Glaukos Investigative Site

Teaneck, New Jersey, United States

Glaukos Investigative Site

Westerville, Ohio, United States