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Completed Phase 3 Interventional Results available

Safety, Efficacy and Pharmacokinetics of OMS302 in Subjects Undergoing Intraocular Lens Replacement With Phacoemulsification

ClinicalTrials.gov ID: NCT01579565

Public ClinicalTrials.gov record NCT01579565. 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, 4:33 AM EDT

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

Official title

A Phase 3 Randomized, Double-Masked, Placebo-Controlled Study of the Pharmacokinetics of OMS302 and the Effect of OMS302 on Intraoperative Pupil Diameter and Early Postoperative Pain in Subjects Undergoing Intraocular Lens Replacement With Phacoemulsification

Study identification

NCT ID
NCT01579565
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Omeros Corporation
Industry
Enrollment
416 participants

Conditions and interventions

Interventions

  • OMS302 Drug
  • Placebo 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
Mar 31, 2012
Primary completion
Oct 31, 2012
Completion
Dec 31, 2012
Last update posted
Jun 13, 2017

2012 – 2013

United States locations

U.S. sites
13
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Not listed Chandler Arizona 85224
Not listed Los Angeles California 90013
Not listed Fort Myers Florida 33901
Not listed Boston Massachusetts 02114
Not listed St Louis Missouri 63131
Not listed Washington Missouri 63090
Not listed Albuquerque New Mexico 87113
Not listed New York New York 10021
Not listed Goodlettsville Tennessee 37072
Not listed Austin Texas 78731
Not listed Houston Texas 77024
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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01579565, 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 Jun 13, 2017 · 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 NCT01579565 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →