Trials / Completed
CompletedNCT01847638
Prolensa (Bromfenac) 0.07% QD vs. Ilevro (Nepafenac) 0.3% QD for Treatment of Ocular Inflammation Post Cataract Surgery
Clinical Outcomes of Prolensa (Bromfenac Ophthalmic Solution) 0.07% QD vs. Ilevro (Nepafenac Ophthalmic Suspension) 0.3% QD for Treatment of Ocular Inflammation Associated With Cataract Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (actual)
- Sponsor
- Melissa Toyos · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To investigate inflammation, visual acuity and macular thickness after treatment with Prolensa vs Ilevro after cataract surgery.
Detailed description
To investigate the clinical outcomes for inflammation, visual acuity and macular thickness after treatment with Prolensa (bromfenac ophthalmic solution) 0.07% QD in subjects who have undergone cataract extraction with posterior chamber intraocular lens implantation.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Prolensa (bromfenac 0.07%) | Comparison of Prolensa (bromfenac ophthalmic solution) 0.07% QD vs. Ilevro (nepafenac ophthalmic suspension) 0.3% QD for Treatment of Ocular Inflammation Associated with Cataract Surgery |
| DRUG | Ilevro (nepafenac 0.3%) | Comparison of Prolensa (bromfenac ophthalmic solution) 0.07% QD vs. Ilevro (nepafenac ophthalmic suspension) 0.3% QD for Treatment of Ocular Inflammation Associated with Cataract Surgery |
Timeline
- Start date
- 2013-04-01
- Primary completion
- 2016-07-16
- Completion
- 2018-08-23
- First posted
- 2013-05-07
- Last updated
- 2018-11-14
- Results posted
- 2018-11-14
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01847638. Inclusion in this directory is not an endorsement.