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Completed Phase 3 Interventional Results available

A Phase 3 Study Evaluating the Efficacy and Safety of OCS-01 Eyedrops Compared to Vehicle for the Treatment of Ocular Inflammation and Pain Following Cataract Surgery

ClinicalTrials.gov ID: NCT05147233

Public ClinicalTrials.gov record NCT05147233. 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, 6:23 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 Eyedrops Compared to Vehicle in the Treatment of Inflammation and Pain Following Cataract Surgery

Brief summary

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

This was a randomized, double-masked, vehicle-controlled, Phase 3 study evaluating the efficacy and safety of OCS-01 QD compared to vehicle in the treatment of inflammation and pain following cataract surgery.

Study identification

NCT ID
NCT05147233
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Oculis
Industry
Enrollment
241 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
Jun 24, 2022 (Actual)
Primary completion
Jun 22, 2023 (Actual)
Completion
Jul 3, 2023 (Actual)
Last update posted
Jul 11, 2025

2022 – 2023

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Oculis Site 16 Chandler Arizona 85224 —
Oculis Site 28 Phoenix Arizona 85003 —
Oculis Site 8 Fayetteville Arkansas 72704 —
Oculis Site 9 Inglewood California 90301 —
Oculis Site 23 Newport Beach California 92663 —
Oculis Site 26 Petaluma California 94954 —
Oculis Site 24 San Pedro California 90731 —
Oculis Site 22 Westminster California 92683 —
Oculis Site 11 Fort Collins Colorado 80528 —
Oculis Site 12 Tamarac Florida 33321 —
Oculis Site 17 Morrow Georgia 30260 —
Oculis Site 20 Louisville Kentucky 40206 —
Oculis Site 5 St Louis Missouri 63128 —
Oculis Site 3 Washington Missouri 63090 —
Oculis Site 13 Kinston North Carolina 28501 —
Oculis Site 6 Brecksville Ohio 44141 —
Oculis Site 14 Cincinnati Ohio 45242 —
Oculis Site 25 Eugene Oregon 97401 —
Oculis Site 7 Kingston Pennsylvania 18704 —
Oculis Site 4 Austin Texas 78731 —
Oculis Site 10 Houston Texas 77025 —
Oculis Site 2 San Antonio Texas 78229 —
Oculis Site 31 San Antonio Texas 78229 —
Oculis Site 27 Salt Lake City Utah 84032 —
Oculis Site 30 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 NCT05147233, 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 Jul 11, 2025 · 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 NCT05147233 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →