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Trials / Completed

CompletedNCT06573606

Ophthalmic Solution in Diabetic Corneal Alteration

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
D&V FARMA srl · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Data analyses and revision of the DED symptoms in diabetic subjects. A novel ophthalmic solution containing cross-linked ha (CX-HA) and Chondroitin sulphate (CS) has been made available on the market. Both molecules have been widely studied for their viscoelastic and hydrating properties. Nevertheless, the use of CS in ophthalmology has been limited since, routinely, the molecule is of animal origins. This new ophthalmic solution is the first on the market formulated with a CS of non-animal origin.

Conditions

Interventions

TypeNameDescription
DEVICECX-HA and CSSterile Isotonic ophthalmic solution

Timeline

Start date
2021-09-01
Primary completion
2022-09-01
Completion
2022-09-01
First posted
2024-08-27
Last updated
2024-08-29

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06573606. Inclusion in this directory is not an endorsement.

Ophthalmic Solution in Diabetic Corneal Alteration (NCT06573606) · Clinical Trials Directory