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Clinical Trial

Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease

NCT: NCT06190054 · COMPLETED

NCT IDNCT06190054
StatusCOMPLETED
Start Date2023-02-06
Completion2025-03-04
SponsorFidia Farmaceutici s.p.a. (INDUSTRY)
First posted
Last updated

Brief Summary

This is a profit, multicentric, prospective, single-arm, open-label, non-pharmacological clinical investigation. Patients with diagnosis of moderate to severe dry eye disease with asthenopia and accommodative effort will receive MERAMIRT®, 1-2 drop per eye 3 times a day for 90 days.

Frequently Asked Questions

What is Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease?

Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease is a clinical trial registered under NCT06190054. Current status: COMPLETED.

What is the status of NCT06190054?

The current status of NCT06190054 (Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease) is: COMPLETED.

When did Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease start?

Evaluation of Performance and Safety of Eye Drops With Hydroxypropyl-methylcellulose and Inositol in Drye Eye Disease started on 2023-02-06.

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Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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