Trials / Completed
CompletedNCT02826421
Clinical Investigation of Corneal Incision Size After Intraocular Lens (IOL) Implantation
Clinical Investigation of Corneal Incision Size After IOL Implantation With Preloaded Delivery Devices and a Manual Delivery Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 114 (actual)
- Sponsor
- Alcon Research · Industry
- Sex
- All
- Age
- 22 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare corneal incision size after IOL implantation with the use of one of four IOL delivery systems (three preloaded IOL delivery systems and one manually loaded IOL delivery system).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | UltraSert Preloaded Delivery System | Includes AcrySof IQ monofocal posterior chamber IOL Model AU00T0, intended for long term use over the lifetime of the subject |
| DEVICE | iTec Preloaded Delivery System | Includes TECNIS 1-piece monofocal IOL, intended for long term use over the lifetime of the subject |
| DEVICE | iSert Preloaded Delivery System | Includes Model 251 or Model 250 posterior chamber IOL, as selected by the Investigator, intended for long term use over the lifetime of the subject |
| DEVICE | Monarch III D Manual IOL Delivery System | Includes AcrySof IQ monofocal IOL posterior chamber IOL Model SN60WF, intended for long term use over the lifetime of the subject |
Timeline
- Start date
- 2016-07-04
- Primary completion
- 2016-11-29
- Completion
- 2016-11-29
- First posted
- 2016-07-11
- Last updated
- 2018-07-02
- Results posted
- 2017-07-28
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT02826421. Inclusion in this directory is not an endorsement.