Trials / Completed
CompletedNCT02246777
Alcon® Ex-PRESS® Glaucoma Filtration Device in Japanese Patients
Assessment of Efficacy and Safety of the EX-PRESS® Glaucoma Filtration Device in Patients With Normal Tension Glaucoma
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to assess the efficacy and safety of the Alcon Ex-PRESS® Glaucoma Filtration Device (Ex-PRESS) in Japanese subjects with normal tension glaucoma.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Ex-PRESS® Glaucoma Filtration Device, Model P50PL |
Timeline
- Start date
- 2014-02-26
- Primary completion
- 2016-10-24
- Completion
- 2016-10-24
- First posted
- 2014-09-23
- Last updated
- 2018-07-20
- Results posted
- 2018-07-20
Locations
1 site across 1 country: Japan
Source: ClinicalTrials.gov record NCT02246777. Inclusion in this directory is not an endorsement.