Trials / Completed
CompletedNCT05579886
Evaluating Two Multifocal Daily Disposable Contact Lenses
Evaluating the Success of Refitting Lens Wearers With MyDay Multifocal, Who Are Already Adapted to Clariti 1Day Multifocal 2-Add Design
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- CooperVision, Inc. · Industry
- Sex
- All
- Age
- 42 Years
- Healthy volunteers
- Not accepted
Summary
The objective of the study was to adapt existing multifocal soft lens wearers to a Control Lens for at least 2 weeks and then evaluate the success of switching them to the Test Lens, with a review after 2 weeks.
Detailed description
This prospective, bilateral eye, open label, non-randomized study compared the performance of 2 different designs of daily disposable multifocal contact lenses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Control Lens | Daily disposable multifocal soft lens with 2 add design (2ADD) for 2 weeks |
| DEVICE | Test Lens | Daily disposable multifocal soft lens with 3 add design (3ADD) for 2 weeks |
Timeline
- Start date
- 2022-10-10
- Primary completion
- 2023-02-07
- Completion
- 2023-02-07
- First posted
- 2022-10-14
- Last updated
- 2024-02-20
- Results posted
- 2024-02-20
Locations
5 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05579886. Inclusion in this directory is not an endorsement.