RecruitingNCT07566975
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
Studying Neurotrophic keratopathy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Neuro-Ophthalmology of Texas
- Principal Investigator
- Rosa A. TangNeuro Ophthalmology of TX
- Intervention
- Cyclosporine ophthalmic solution 0.1%(other)
- Enrollment
- 50 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2026 – 2026
Study locations (1)
- Neuro Ophthalmology of TX, Houston, Texas, United States
Collaborators
Harrow Inc
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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