Trials / Completed
CompletedNCT04743622
Comparison of Efficacy and Ocular Surface Disease Assessment Between Monoprost and BAK-preserved Latanoprost
Comparison of Efficacy and Ocular Surface Disease Assessment Between Monoprost and BAK-preserved Latanoprost in Glaucoma or Ocular Hypertensive Patients
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 57 (actual)
- Sponsor
- CHA University · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
Summary
Comparison of Efficacy and Ocular Surface Disease Assessment Between Monoprost and BAK-preserved Latanoprost in Glaucoma or Ocular Hypertensive Patients : Phase 4, Parallel Group Design, Investigator-blind, Active-control, Randomized, Multi-center Study
Detailed description
Not provided
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Monoprost | preservative-free latanoprost 1 drop once a day for 12 weeks to target eyes |
| DRUG | Xalatan | preserved latanoprost 1 drop once a day for 12 weeks to target eyes |
Timeline
- Start date
- 2019-04-30
- Primary completion
- 2020-06-23
- Completion
- 2020-09-13
- First posted
- 2021-02-08
- Last updated
- 2021-02-08
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT04743622. Inclusion in this directory is not an endorsement.