Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients

Completed · Phase 4

Conditions studied: Cataract

In brief

Evaluation of the aqueous concentrations of 2 topical NSAIDS as well as the PGE2 inhibition in human patients.

Key facts

Study ID

NCT00347503

Run by

Innovative Medical

Last updated by the study team

2007-07-13

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Healthy Male/Female 21 years of age of older.
• Patient understands and is willing to sign the written informed consent form
• Likely to complete the entire course of the study.
• Patient is scheduled to undergo cataract surgery
• Female patients of childbearing potential must have had a regular menstrual cycle prior to study entry (a female is considered of childbearing potential unless she is postmenopausal, without a uterus and/or both ovaries, or has had a bilateral tubal ligation).
• Patient is willing and able to administer eye drops and record the times the drops were instilled

You may not qualify if…

• Patient has been using a topical NSAID within 1 week of study entry
• Patient has a known sensitivity to any of the ingredients in the study medications
• Patient has sight in only one eye
• Patient has a history of previous intraocular surgery
• Patient's doctor has determined they have a condition (i.e., UNCONTROLLED systemic disease) or are in a situation that may put them at significant risk, confound the study results or may interfere significantly with their participation in the study
• Female patients who are pregnant, nursing an infant or planning a pregnancy
• Patients who are currently involved in another investigational study or have participated in one within the 30 days prior to entering this study

Where it is running

• Bucci Laser Vision — Wilkes-Barre, Pennsylvania, United States

Full record on ClinicalTrials.gov

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