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Completed Phase 2 Interventional Results available

Safety and Efficacy of OMS302 in Subjects Undergoing Unilateral Cataract Extraction With Lens Replacement (CELR)

ClinicalTrials.gov ID: NCT01193127

Public ClinicalTrials.gov record NCT01193127. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 7:21 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine whether the use of OMS302 (the study drug) in individuals undergoing Cataract Extraction with Lens Replacement (CELR) surgery is safe and effective at maintaining an adequately dilated pupil during surgery and reducing post-operative symptoms of discomfort (such as eye pain and irritation).

Study identification

NCT ID
NCT01193127
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Omeros Corporation
Industry
Enrollment
223 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 2010 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Feb 2011 (Actual)
Last update posted
Aug 28, 2014

2010 – 2011

United States locations

U.S. sites
24
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Not listed Chandler Arizona 85224 —
Not listed Glendale Arizona 85308 —
Not listed Little Rock Arkansas 72205 —
Not listed Los Angeles California 90013 —
Not listed Parker Colorado 80134 —
Not listed Largo Florida 33770 —
Not listed North Fort Myers Florida 33903 —
Not listed Panama City Florida 32405 —
Not listed Tamarac Florida 33321 —
Not listed Gurnee Illinois 60031 —
Not listed Gretna Louisiana 70056 —
Not listed Kansas City Missouri 64111 —
Not listed St Louis Missouri 63131 —
Not listed Omaha Nebraska 68131 —
Not listed Las Vegas Nevada 89135 —
Not listed Albuquerque New Mexico 87113 —
Not listed Rockville Centre New York 11570 —
Not listed Bala-Cynwyd Pennsylvania 19004 —
Not listed Goodlettsville Tennessee 37072 —
Not listed Austin Texas 78731 —
Not listed Houston Texas 77024 —
Not listed Nacogdoches Texas 75965 —
Not listed San Antonio Texas 78229 —
Not listed Salt Lake City Utah 84132 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01193127, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 28, 2014 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01193127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →