A Randomized Study in Children Ages Birth Through Three Years Undergoing Unilateral Cataract Extraction With or Without Lens Replacement

Completed · Phase 3

Conditions studied: Unilateral Cataract Extraction, Congenital Cataract

In brief

The purpose of this study is to evaluate the effect of OMS302 compared to phenylephrine when administered in irrigation solution during cataract extraction on intraoperative pupil diameter, acute postoperative pain, and safety in children birth through 3 years.

Key facts

Study ID

NCT02132312

Run by

Omeros Corporation

People needed

78

Starts

2014-07-01

Expected to finish

2016-09-12

Last updated by the study team

2021-07-22

Who can join

Age: 0 and older, up to 4. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Are 0 through three years of age at the time of surgery.
• Are to undergo unilateral primary cataract extraction with or without lens replacement.
• Have informed consent and Health Insurance Portability and Accountability Act (HIPAA) Authorization provided by a parent or legal guardian in accordance with local regulations and governing IRB/IEC requirements prior to any procedures or evaluations performed specifically for the sole purpose of this study.
• A parent or legal guardian has indicated that they understand and are able, willing, and likely to fully comply with study procedures and restrictions.

You may not qualify if…

• Corneal diameter less than nine millimeters in the study eye.
• Hypersensitivity to phenylephrine, ketorolac, or other NSAIDs, including aspirin, or latex.
• Surgeon's expectation that the protocol-specified mydriatic regimen will not be adequate to perform the procedure and that additional mydriatic treatment (pharmacological or mechanical) will be required.
• Presence of clinically significant gastrointestinal, cardiovascular, hepatic, renal, hematological, endocrine, neurological, psychiatric, respiratory, or other medical condition that could increase the risk to the subject as determined by the Investigator.
• Presence of active or suspected viral, bacterial, or fungal disease in the study eye.
• Use of any topical medication in the study eye within seven days prior to surgery, except for medications needed to examine the eye or prepare for surgery.
• Have a post-traumatic cataract.
• History of uveitis or evidence of past uveitis such as synechiae or keratic precipitates in the study eye.
• Have an ocular neoplasm in the study eye.
• Have a clinically significant infection.
• Have suspected permanent or low vision in the fellow non-study eye, unless caused by a cataract. The study eye must not be the subject's only good eye.
• Use of systemic corticosteroids or NSAIDs in the seven days prior to surgery.
• Have a history of clinically significant corticosteroid-induced intraocular pressure increase.
• Use of any medication for ocular hypertension or glaucoma in the study eye.
• Use of monoamine oxidase inhibitors for 21 days preoperatively.
• Prior participation in a clinical study of OMS302.
• Participating in any investigational drug or device trial within the 30 days prior to the day of surgery.
• History of intraocular non-laser surgery in the study eye within the three months prior to the day of surgery, or intraocular laser surgery in the study eye within 30 days prior to the day of surgery.
• Presence of any condition that the Investigator believes would put the subject at risk or confound the interpretation of the study data.
• Be a member of the immediate family of the Investigator or employees of the investigative site. Immediate family is defined as the Investigator's or employees' natural or legally adopted child (including a stepchild living in the Investigator's household), or grandchild.

Where it is running

• Study site — Los Angeles, California, United States
• Study site — Atlanta, Georgia, United States
• Study site — Chicago, Illinois, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Kansas City, Kansas, United States
• Study site — Boston, Massachusetts, United States
• Study site — Detroit, Michigan, United States
• Study site — Charleston, North Carolina, United States
• Study site — Nashville, Tennessee, United States
• Study site — Dallas, Texas, United States
• Study site — Madison, Wisconsin, United States

Full record on ClinicalTrials.gov

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