ClinicalTrials.gov record
Completed Phase 3 Interventional

Safety and Efficacy of 0.75% Phentolamine Ophthalmic Solution in Subjects With Post-refractive Surgery Visual Disturbances

ClinicalTrials.gov ID: NCT06349759

Public ClinicalTrials.gov record NCT06349759. 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 May 20, 2026, 10:02 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

Randomized, Placebo-Controlled, Double-Masked Study of the Safety and Efficacy of POS (0.75% Phentolamine Ophthalmic Solution) in Subjects Who Have Previously Had Keratorefractive Surgery and Have Decreased Visual Acuity Under Mesopic Conditions

Study identification

NCT ID
NCT06349759
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ocuphire Pharma, Inc.
Industry
Enrollment
200 participants

Conditions and interventions

Interventions

  • Placebo Drug
  • phentolamine ophthalmic solution 0.75%, a non-selective alpha-1 and alpha-2 adrenergic antagonist 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, 2024
Primary completion
Apr 16, 2025
Completion
Feb 18, 2026
Last update posted
Mar 11, 2026

2024 – 2026

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
23
Facility City State ZIP Site status
United States Phoenix Pheonix Arizona 85003
United States Scottsdale Scottsdale Arizona 85260
United States Bakersfield California 93309
United States, Glendale, CA Glendale California 91204
United States, LaJolla, CA La Jolla California 92903
United States, California Newport Beach California 92663
United States Rowland Heights Rowland Heights California 91748
United States Torrance Torrance California 90505
United States, Jacksonville, FL Jacksonville Florida 32256
United States Jacksonville Jacksonville Florida 32257
United States Tampa Florida 33603
United States Overland Park Overland Park Kansas 66210
United States Louisville Louisville Kentucky 40206
United States Fraser Fraser Michigan 48026
United States New York New York 10022
United States Smithtown Smithtown New York 11787
United States, North Carolina Garner North Carolina 27529
United States Fargo Fargo North Dakota 58103
United States Fargo North Dakota 58103
United States, Rhode Island Warwick Rhode Island 02888
United States, Mt Pleasant, SC Mt. Pleasant South Carolina 29464
United States Chattanooga Chattanooga Tennessee 37411
United States Smyrna Smyrna Tennessee 37167
United States Draper Draper Utah 84020
United States Lynchburg 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 NCT06349759, 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 Mar 11, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06349759 live on ClinicalTrials.gov.

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