Trials / Completed
CompletedNCT04175340
A Safety and Effectiveness Study of a New Preservative Free Rewetting Drop
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 369 (actual)
- Sponsor
- Bausch & Lomb Incorporated · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The objective of this study is to evaluate the safety and effectiveness of lubricating and rewetting drop (Test) compared to OPTI-FREE® Replenish® Rewetting Drops (Control) when used by habitual contact lens wearers to bilaterally lubricate and rewet soft (hydrophilic) contact lenses including silicone hydrogel contact lenses and gas permeable (silicone acrylate and fluoro silicone acrylate) contact lenses.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | BL-300-PFM04 | Preservative Free Lubricating and Rewetting Drops for use during contact lens wear |
| DEVICE | OPTI-FREE | Replenish Rewetting Drops |
Timeline
- Start date
- 2019-11-07
- Primary completion
- 2020-02-17
- Completion
- 2020-02-17
- First posted
- 2019-11-25
- Last updated
- 2024-07-10
- Results posted
- 2024-07-10
Locations
15 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT04175340. Inclusion in this directory is not an endorsement.