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Investigation of Preservative-Free Ophthalmic Solution in Ocular Dryness

NCT05778942 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2024-02-06

No results posted yet for this study

Summary

This is a multicenter, prospective, observational, open-label, non-interventional study evaluating the clinical performance and the safety of 4 daily instillations of the ophthalmic solution in the treatment of eye discomfort, in particular due to eye dryness

Conditions

  • Dry Eye Syndromes

Interventions

DEVICE

Eyestil SYNFO

Instillation of study drug in both eyes: preservative-free ophthalmic solution based on sodium hyaluronate and xanthan gum

Sponsors & Collaborators

  • SIFI SpA

    lead INDUSTRY

Principal Investigators

  • Claudine Civiale · SIFI S.p.A.

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-02-23
Primary Completion
2023-11-06
Completion
2023-12-19

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05778942 on ClinicalTrials.gov