Trials / Withdrawn
WithdrawnNCT00758940
Clinical Assessment of Visual Function With the Acrysof ReSTOR Multifocal IOL
A Six-months, Open-labelled Clinical Assessment of Visual Function After Bilateral Implantation of Arcysof ReSTOR Multifocal Intra-ocular Lens
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
Summary
An unmasked trial after bilateral implantation of AcrySof® ReSTOR®, SA60D3 IOL . Enrolled are at least 30 patients or as much as possible from the doctor's clinical practice perspective. 6 months follow-up after IOL implant in the 2nd eye
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Acrysof ReSTOR multifocal IOL | Implanted into the study eye following cataract extraction surgery |
Timeline
- First posted
- 2008-09-25
- Last updated
- 2015-05-12
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00758940. Inclusion in this directory is not an endorsement.