Trials / Completed
CompletedNCT02566083
Post-Approval Study of the Tecnis® Toric IOL
Post-Approval Study of the Tecnis® Toric IOL, Models ZCT300 and ZCT400
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 365 (actual)
- Sponsor
- Abbott Medical Optics · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
This study is a prospective, multicenter, bilateral, non-randomized, open-label, comparative clinical study conducted at up to 80 sites in the USA. Subjects will choose to be bilaterally implanted with either 1) the TECNIS 1-Piece Toric IOLs, Model ZCT300 and/or ZCT400, or 2) the TECNIS Monofocal Model ZCB00 non-toric control IOL, according to subject preference
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | non-toric intraocular lens | TECNIS One-piece Monofocal Model ZCB00 |
| DEVICE | toric intraocular lens | TECNIS One-piece Toric Models ZCT300 or ZCT400 |
Timeline
- Start date
- 2015-10-21
- Primary completion
- 2018-12-11
- Completion
- 2019-05-23
- First posted
- 2015-10-01
- Last updated
- 2020-01-18
- Results posted
- 2020-01-18
Locations
44 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02566083. Inclusion in this directory is not an endorsement.