Trials / Terminated
TerminatedNCT01249144
Visual and Refractive Outcomes After Implantation of Aspheric IOLs With Different Dioptric Increments and Manufacturing
A Randomized Fellow-eye Controlled Clinical Trial to Compare the Visual and Refractive Outcomes Between Two Aspheric IOLs With Different Dioptric Increments and Manufacturing Tolerances in Patients Undergoing Bilateral Cataract Surgery
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 75 (actual)
- Sponsor
- Lenstec Incorporated · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
This study compares two intraocular lenses, the Softec HD and the Tecnis Z9002, used to replace the natural crystalline lens after cataract extraction. The variables compared include 1) the accuracy of targeted versus achieved refractive outcomes and 2) visual acuity outcomes three months after implantation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intraocular Lens (IOL) | Device for implantation in the capsular bag of the eye for visual correction of aphakia following cataract surgery. |
Timeline
- Start date
- 2010-10-01
- Primary completion
- 2012-01-01
- Completion
- 2012-01-01
- First posted
- 2010-11-29
- Last updated
- 2018-10-18
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01249144. Inclusion in this directory is not an endorsement.