Clinical Trials Directory

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UnknownNCT06172530

Observational Study on the Improvement of Dry Eye Syndrome, Treatment Satisfaction, and Intraocular Tolerance With Diquasol Eye Drops

Observational Study on the Improvement of Dry Eye Syndrome, Treatment Satisfaction, and Intraocular Tolerance With Diquasol Eye Drops and Hyaluron/Hyaluronmax Eye Drops in Patients Over 19 Years Old With Dry Eye Syndrome

Status
Unknown
Phase
Study type
Observational
Enrollment
2,000 (estimated)
Sponsor
Hanlim Pharm. Co., Ltd. · Industry
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

This study is to verify the efficacy and safety in the treatment of dry eye syndrome in patients prescribed with Diquasol eye drops as a monotherapy, or in combination with Hyaluron eye drops, or in combination with Hyaluronmax eye drops.

Detailed description

This study is to observe the prescription patterns in routine clinical practice and assess the changes in dry eye symptoms, treatment satisfaction, and intraocular tolerance over a 12-week period in patients prescribed with Diquasol eye drops as a monotherapy or in combination with Hyaluron eye drops or Hyaluronmax eye drops for the treatment of dry eye syndrome.

Conditions

Timeline

Start date
2023-02-08
Primary completion
2024-05-01
Completion
2024-12-01
First posted
2023-12-15
Last updated
2023-12-15

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT06172530. Inclusion in this directory is not an endorsement.