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Not Yet RecruitingNCT07457021

A Study to Evaluate the Safety and Effectiveness of Perfluorohexyloctane Eye Drops on Treatment of Dry Eye Disease (DED) Related to Meibomian Gland Dysfunction (MGD)

Treating Dry Eye Disease Related to Meibomian Gland Dysfunction With Perfluorohexyloctane Eye Drops : A Prospective, Multicenter, Real-world Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
2,000 (estimated)
Sponsor
Xiamen Ophthalmology Center Affiliated to Xiamen University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Perfluorohexyloctane eye drops is the only drug in China approved for treating Dry Eye Disease (DED) related to Meibomian Gland Dysfunction (MGD), its efficacy and safety in the clinical practice of treating DED related to MGD in the real world, whether in combination with or without various other treatment methods (other drugs or physical therapy) , remain to be explored. This study aims to collect data on the treatment of DED related to MGD with perfluorohexyloctane under real medical conditions. Through analysis, it seeks to obtain clinical evidence of the product's application value and potential benefits or risks, providing evidence for the treatment of DED elated to MGD with perfluorohexyloctane under real medical conditions.

Conditions

Timeline

Start date
2026-03-01
Primary completion
2028-08-31
Completion
2029-09-30
First posted
2026-03-09
Last updated
2026-03-09

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07457021. Inclusion in this directory is not an endorsement.

A Study to Evaluate the Safety and Effectiveness of Perfluorohexyloctane Eye Drops on Treatment of Dry Eye Disease (DED) (NCT07457021) · Clinical Trials Directory