Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery
Primary Purpose
Cataract
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
bromfenac ophthalmic solution
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Cataract focused on measuring Cataract extraction with intraocular lens implantation
Eligibility Criteria
Inclusion Criteria:
- Scheduled for cataract surgery
Exclusion Criteria:
- Known hypersensitivity to bromfenac and salicylates
Sites / Locations
- ISTA Pharmaceuticals, Inc.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Bromfenac
Placebo
Arm Description
Bromfenac Ophthalmic Solution 0.09%, Dosed 1 Drop Daily
Placebo, Dosed 1 Drop Daily
Outcomes
Primary Outcome Measures
Number of Participants With Summed Ocular Inflammation Score (SOIS) of Zero
Participants with SOIS of 0. Scale: 0=0 cells (complete absence); 0.5=1-5 cells (trace); 1=6-15 cells (very slight); 2=16-25 cells (moderate); 3=26-50 cells (marked); 4=>50 cells (intense)
Secondary Outcome Measures
Number of Participants That Are Pain Free
Participant description of being pain free taken from patient questionnaire with multiple possible responses (None, Mild, Moderate, Severe) within one hour of instilling eye drop
Full Information
NCT ID
NCT00703781
First Posted
June 20, 2008
Last Updated
March 4, 2015
Sponsor
Bausch & Lomb Incorporated
1. Study Identification
Unique Protocol Identification Number
NCT00703781
Brief Title
Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
June 2008 (undefined)
Primary Completion Date
November 2008 (Actual)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Bausch & Lomb Incorporated
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract
Keywords
Cataract extraction with intraocular lens implantation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
126 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Bromfenac
Arm Type
Experimental
Arm Description
Bromfenac Ophthalmic Solution 0.09%, Dosed 1 Drop Daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo, Dosed 1 Drop Daily
Intervention Type
Drug
Intervention Name(s)
bromfenac ophthalmic solution
Intervention Description
sterile ophthalmic solution
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
sterile ophthalmic solution
Primary Outcome Measure Information:
Title
Number of Participants With Summed Ocular Inflammation Score (SOIS) of Zero
Description
Participants with SOIS of 0. Scale: 0=0 cells (complete absence); 0.5=1-5 cells (trace); 1=6-15 cells (very slight); 2=16-25 cells (moderate); 3=26-50 cells (marked); 4=>50 cells (intense)
Time Frame
Day 15
Secondary Outcome Measure Information:
Title
Number of Participants That Are Pain Free
Description
Participant description of being pain free taken from patient questionnaire with multiple possible responses (None, Mild, Moderate, Severe) within one hour of instilling eye drop
Time Frame
Day 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Scheduled for cataract surgery
Exclusion Criteria:
Known hypersensitivity to bromfenac and salicylates
Facility Information:
Facility Name
ISTA Pharmaceuticals, Inc.
City
Irvine
State/Province
California
ZIP/Postal Code
92618
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Efficacy and Safety of Bromfenac Ophthalmic Solution in Cataract Surgery
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