Trials / Withdrawn
WithdrawnNCT00708331
Hydrophilic Acrylic Intraocular Lens
SC25-FOLD Hydrophilic Acrylic Intraocular Lens
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- EyeKon Medical, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the safety and efficacy of Hydrophilic Acrylic Intraocular Lens after cataract surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | 2 HEMA Hydrophilic Acrylic Intraocular Lens | 2 HEMA Hydrophilic Acrylic Intraocular Lens implanted into the posterior capsule following cataract surgery for patient life duration. |
Timeline
- Start date
- 2002-08-01
- Primary completion
- 2007-05-01
- First posted
- 2008-07-02
- Last updated
- 2021-02-03
Locations
9 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00708331. Inclusion in this directory is not an endorsement.