Clinical Trials Directory

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

TypeNameDescription
DRUGXibrom, and OptiveXibrom: two drops a day, three days before surgery and 21 days after surgery. Optive: three times a day for 21 days after surgery.
DRUGXibrom and Pred ForteXibrom: 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.