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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00524264
Other study ID # 191578-005
Secondary ID
Status Completed
Phase Phase 3
First received August 30, 2007
Last updated September 29, 2009
Start date October 2007
Est. completion date April 2008

Study information

Verified date August 2009
Source Allergan
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a 16-day study to evaluate the safety and efficacy of ketorolac eye drops for the treatment of inflammation and pain associated with cataract surgery.


Recruitment information / eligibility

Status Completed
Enrollment 248
Est. completion date April 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients undergoing cataract surgery

Exclusion Criteria:

- Uncontrolled ocular disease in cataract surgery eye

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
ketorolac
Ophthalmic drops, BID pre- and post-operation, and 6 doses on surgery day. Placebo

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Allergan

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Resolution of Post Operative Inflammation Day 14 No
Secondary Ocular Pain Day 1 No
Secondary Mean Pupil Area Day 0 No
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