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Four-Week Ocular-Surface Evaluation of an Experimental Ophthalmic Liposomal Nanocarrier in Dry Eye Disease
Sponsor: Regional Specialist Hospital in Wroclaw
Summary
This prospective, single-group research medical experiment evaluated the ocular-surface response to repeated bilateral use of an experimental ophthalmic liposomal nanocarrier in adults with dry eye disease. Participants used one drop in each eye three times daily (morning, midday, and evening) for four weeks. Clinical assessments were performed at baseline and follow-up and included ocular-surface staining, tear-film stability, tear-volume measures, symptoms, and contextual ophthalmic measures. A nested optical assessment evaluated tear-film surface regularity and non-invasive tear-film parameters.
Official title: A Prospective Single-Group Research Medical Experiment Evaluating Four-Week Ocular-Surface and Tear-Film Response to an Experimental Ophthalmic Liposomal Nanocarrier in Adults With Dry Eye Disease
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
26
Start Date
2022-03-17
Completion Date
2022-06-30
Last Updated
2026-08-28
Healthy Volunteers
No
Conditions
Interventions
Experimental ophthalmic liposomal nanocarrier
One drop was instilled into each eye three times daily (morning, midday, and evening) for four weeks.
Locations (1)
Regional Specialist Hospital in Wroclaw
Wroclaw, Poland