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
Part of paid clinical trials in Houston, Texas.
- Sponsor
- Neuro-Ophthalmology of Texas
- Study ID
- NCT07566975
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Cyclosporine ophthalmic solution 0.1% — OTHERone drop in both eyes twice a day
Study Details
patients from a Neuro Ophthalmology who have dry eye, some of which have neurotrophic keratitis are being analyzed after treatment with Vevye
Key Dates
- Start date
- Mar 31, 2026
- Status verified
- Apr 2026
- Primary completion
- Nov 30, 2026
- Completion
- Nov 30, 2026
Study Design
- Enrollment
- 50 participants (estimated)
Arms
- Arm: Dry Eye without neurotrophic changes
- Arm: Dry Eye with neurotrophic changes
Primary Outcome Measure
Corneal fluorescein staining [ Time Frame: Baseline compared to week 4 ]
Central Contacts
- Laura Perez12817238593
- Rosa A Tang, MD713-258-0009
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Neuro Ophthalmology of TX | Houston | Texas | 77074 |
Find similar trials in Houston, TX
By research site
Related Studies
- Low Level Light Therapy & Skin PigmentationRecruiting · University of Houston · Houston, Texas
- Penn SICCA Follow-up StudyNot Yet Recruiting · University of Pennsylvania · Philadelphia, Pennsylvania
- Use of Acthar Gel Single-Dose Pre-Filled SelfJectTM Injector in Patients With Moderate-Severe Keratitis and Autoimmune DiseasePHASE4 · Recruiting · Toyos Clinic · Nashville, Tennessee
- Quality of Life in Presbyopic Patients Who Are Treated With QlosiPHASE4 · Recruiting · Southern College of Optometry · Medina, Minnesota