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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 Jul 22, 2026, 12:08 PM EDT

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

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

Conditions

Interventions

  • OMS302 Solution Drug
  • OMS302 Mydriatic Solution Drug
  • OMS302 Anti-inflammatory Solution Drug
  • Balanced Salt Solution (BSS) Solution Drug

Drug

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
Jun 30, 2010
Primary completion
Dec 31, 2010
Completion
Jan 31, 2011
Last update posted
Aug 27, 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 27, 2014 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01193127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →