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Terminated Phase 3 Interventional

Study Evaluating the Efficacy and Safety of OCS-01 Eye Drops in Subjects Following Cataract Surgery

ClinicalTrials.gov ID: NCT06128369

Public ClinicalTrials.gov record NCT06128369. 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 21, 2026, 4:50 PM 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 Randomized, Double-masked, Vehicle-controlled Study Evaluating the Efficacy and Safety of OCS-01 Ophthalmic Suspension in the Treatment of Inflammation and Pain Following Cataract Surgery

Study identification

NCT ID
NCT06128369
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Oculis
Industry
Enrollment
117 participants

Conditions and interventions

Interventions

  • Dexamethasone Ophthalmic Suspension Drug
  • Vehicle of OCS-01 Other

Drug · Other

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
Dec 17, 2023
Primary completion
May 1, 2024
Completion
May 8, 2024
Last update posted
Dec 9, 2024

2023 – 2024

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Oculis Investigative Site Inglewood California 90301
Oculis Investigative Site Morrow Georgia 30260
Oculis Investigative Site Louisville Kentucky 40206
Oculis Investigative Site St Louis Missouri 63131
Oculis Investigative Site Washington Missouri 63090
Oculis Investigative Site Elizabeth City North Carolina 27909
Oculis Investigative Site Eugene Oregon 97401
Oculis Investigative Site Kingston Pennsylvania 18704
Oculis Investigative Site Austin Texas 78731
Oculis Investigative Site Houston Texas 77008
Oculis Investigative Site San Antonio Texas 78229
Oculis Investigative Site Lynchburg Virginia 24502

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 NCT06128369, 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 Dec 9, 2024 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06128369 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →