Trials / Unknown
UnknownNCT01860612
Safety and Effectiveness of the CustomFlex Artificial Iris Prosthesis for the Treatment of Iris Defects
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 500 (estimated)
- Sponsor
- Clinical Research Consultants, Inc. · Industry
- Sex
- All
- Age
- 3 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to study the long term safety and effectiveness of an artificial iris prosthesis for the treatment of iris defects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Artificial Iris (CustomFlex) |
Timeline
- Start date
- 2013-10-01
- Primary completion
- 2025-12-31
- Completion
- 2025-12-31
- First posted
- 2013-05-23
- Last updated
- 2022-10-24
Locations
13 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT01860612. Inclusion in this directory is not an endorsement.