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

Innovative Medical2 个研究点分布在 1 个国家开始时间: 2006年7月4日最近更新: 2007年7月13日

适应症

试验速览

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

•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

•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

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