Trials / Completed
CompletedNCT00698724
Comparing Optical Coherence Tomography (OCT) and Visual Acuity Outcomes in Subjects Undergoing Cataract Surgery, Who Receive Xibrom Ophthalmic Solution and Standard Presurgical Care vs. Xibrom Ophthalmic Solution Plus Prednisolone Acetate 1% and Standard Presurgical Care
A Prospective, Randomized Single-Masked Clinical Trial Comparing OCT and Visual Acuity Outcomes in Subjects Undergoing Cataract Surgery, Who Receive Xibrom Ophthalmic Solution and Standard Presurgical Care vs. Xibrom Ophthalmic Solution Plus Prednisolone Acetate 1% and Standard Presurgical Care
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Bp Consulting, Inc · Network
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To compare the efficacy of twice-daily topical bromfenac (Xibrom) ophthalmic solution alone versus twice-daily topical Xibrom with prednisolone acetate 1% three-times daily on visual acuity and OCT measurements.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Xibrom, and Optive | Xibrom: two drops a day, three days before surgery and 21 days after surgery. Optive: three times a day for 21 days after surgery. |
| DRUG | Xibrom and Pred Forte | Xibrom: two drops a day, three days before surgery and 21 days after surgery. Pred Forte: three times a day for 21 days after surgery. |
Timeline
- Start date
- 2008-06-01
- Primary completion
- 2009-06-01
- Completion
- 2009-06-01
- First posted
- 2008-06-17
- Last updated
- 2009-06-10
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00698724. Inclusion in this directory is not an endorsement.