Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

Study to See How Well an Eye Drop, SURF-201, Works and What Side Effects There Are in Cataract Surgery Subjects

ClinicalTrials.gov ID: NCT04324359

Public ClinicalTrials.gov record NCT04324359. 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 Sep 9, 2026, 12:33 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 Multicenter, Randomized, Double-Masked Study To Compare The Ocular Safety, Tolerability, And Efficacy Of A Topical 0.2% Ophthalmic Corticosteroid Solution (SURF-201) To Vehicle In Cataract Surgery Subjects

Brief summary

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

SURF-201 is being studied for the treatment of eye inflammation and pain in people who are undergoing cataract surgery. SURF-201 is an investigational drug (which means the study drug is currently being tested) in the form of a sterile eye drop. The purpose of this research study is to see how well SURF-201 works and what side effects there are, and to compare it with Vehicle (placebo). This study will involve about 80 study participants at several different research sites in the United States.

Study identification

NCT ID
NCT04324359
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Surface Ophthalmics, Inc.
Industry
Enrollment
91 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
Mar 2, 2020
Primary completion
Nov 2, 2020
Completion
Nov 19, 2020
Last update posted
Jan 14, 2025

2020

United States locations

U.S. sites
10
U.S. states
6
U.S. cities
10
Facility City State ZIP Site status
Inland Eye Specialists Hemet California 92545
LoBue Laser and Eye Medical Center Murrieta California 92562
Hernando Eye Institute Brooksville Florida 34613
Levenson Eye Associates Jacksonville Florida 32204
East Florida Eye Institute Stuart Florida 34994
Alterman, Modi & Wolter Poughkeepsie New York 12603
Eye Care Specialists Kingston Pennsylvania 18704
VRF Eye Specialty Group Memphis Tennessee 38120
Texan Eye Care, PA - Keystone Research, Ltd. Austin Texas 78731
R and R Eye Research, LLC San Antonio Texas 78229

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 NCT04324359, 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 Jan 14, 2025 · Synced Sep 9, 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 NCT04324359 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →