Actively Recruiting

Age: 18Years +
All Genders
NCT07566975

Real-World Assessment of VEVYE® for Short-Term Symptom and Sign Improvement of Dry Eye Disease in a Neuro-Ophthalmology Clinic: A 6-Month Prospective Observational Study

Led by Neuro-Ophthalmology of Texas · Updated on 2026-05-05

50

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

Sponsors

N

Neuro-Ophthalmology of Texas

Lead Sponsor

H

Harrow Inc

Collaborating Sponsor

AI-Summary

What this Trial Is About

patients from a Neuro Ophthalmology who have dry eye, some of which have neurotrophic keratitis are being analyzed after treatment with Vevye

CONDITIONS

Official Title

Real-World Assessment of VEVYE® for Short-Term Symptom and Sign Improvement of Dry Eye Disease in a Neuro-Ophthalmology Clinic: A 6-Month Prospective Observational Study

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosis of neuro-ophthalmic condition
  • Clinical diagnosis of dry eye disease
  • Ocular Surface Disease Index (OSDI) score of 23 or greater at baseline
  • Presence of an objective sign of dry eye disease
  • Indicated for VEVYE prior to enrollment
  • Ability and willingness to complete study visits and questionnaires
Not Eligible

You will not qualify if you...

  • Presence of a corneal ulcer
  • Use of another cyclosporine or lifitegrast product within 30 days before baseline
  • Ocular surgery within 30 days prior to baseline
  • Active ocular infection or severe ocular surface condition unrelated to dry eye disease
  • Contact lens wearers (must be off contacts for 30 days before and during the trial)
  • Any condition that prevents compliance or informed consent
  • Subjects with severe scarring or zero corneal sensitivity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Neuro Ophthalmology of TX

Houston, Texas, United States, 77074

Actively Recruiting

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Research Team

L

Laura Perez

CONTACT

R

Rosa A Tang, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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