CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 20 enrolled
Drug / intervention
CX-HA and CSdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06573606
NCT06573606N/ACompleted

Ophthalmic Solution in Diabetic Corneal Alteration

D&V FARMA srl·observational·Posted Aug 27, 2024·Updated Aug 29, 2024

In Brief

An observational study evaluating CX-HA and CS for Dry Eye Disease (DED). Completed, enrolled 20 participants across 1 site.

Detailed 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.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesItaly

Timeline

N/ACompletedFinished
20222023202420252026
First PostedAug 27, 2024
Enrollment StartSep 1, 2021
Primary CompletionSep 1, 2022
TodayJul 2, 2026
Enrollment to primary: 1 yearPosted 1.8 years ago

Interventions

CX-HA and CSdevice

Sterile Isotonic ophthalmic solution