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Active, not recruiting Phase 3 Interventional

OPI-NXYDLD-303 Safety and Efficacy of Phentolamine Ophthalmic Solution in Keratorefractive Surgery Participants With Decreased Mesopic Visual Acuity

ClinicalTrials.gov ID: NCT07140783

Public ClinicalTrials.gov record NCT07140783. 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 6, 2026, 2:29 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

RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-MASKED STUDY OF THE SAFETY AND EFFICACY OF POS (0.75% PHENTOLAMINE OPHTHALMIC SOLUTION) IN PARTICIPANTS WITH PREVIOUS KERATOREFRACTIVE SURGERY WITH DECREASED VISUAL ACUITY UNDER MESOPIC CONDITIONS

Brief summary

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

The goal of this clinical trial is to learn if Phentolamine Ophthalmic Solution works to treat adults that have had keratorefractive surgery and have decreased visual acuity under mesopic conditions. It will also learn about the safety of Phentolamine Ophthalmic Solution. The main questions it aims to answer are: Researchers will compare Phentolamine Ophthalmic Solution to a placebo (a look-alike substance that contains no drug) to see if Phentolamine Ophthalmic Solution works to improve vision in low light conditions. Participants will: Take Phentolamine Ophthalmic Solution or a placebo drop every day for 2 weeks Visit the clinic once every week for 2 weeks for checkups and tests Keep a diary of when they instill the study medication each evening

Study identification

NCT ID
NCT07140783
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Ocuphire Pharma, Inc.
Industry
Enrollment
200 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
Sep 1, 2025
Primary completion
May 31, 2026
Completion
May 31, 2026
Last update posted
Jun 21, 2026

2025 – 2026

United States locations

U.S. sites
23
U.S. states
10
U.S. cities
21
Facility City State ZIP Site status
Arizona Eye Care Chandler Arizona 85224
Carrot Eye Center Mesa Arizona 85202
Eye Doctors of Arizona Phoenix Arizona 85028
MRB Eye Care Consultants Scottsdale Arizona 85254
Global Research Management Glendale California 91204
Gordon Schanzlin New Vision La Jolla California 92037
Eye Research Foundation Newport Beach California 92663
California Eye Specialists Medical Group Pasadena California 91107
NVISION Clinical Research San Diego California 92117
Scripps Poway Eyecare and Optometry San Diego California 92130
Wolsten and Goldberg Eye Assoc. Torrance California 90505
Glaucoma Specialist of South Florida Delray Beach Florida 33484
Segal Drug Trials Delray Beach Florida 33484
Wyse Eyecare Northbrook Illinois 60062
Virdi Eye Clinic Rock Island Illinois 61201
Durrie Vision Overland Park Kansas 66210
Kannarr Eye Care Pittsburg Kansas 66762
Eye Health Vision Center Russells Mills Massachusetts 02747
Northeast Eye Research Associates Woburn Massachusetts 01801
Oculus Research Garner North Carolina 27529
West Bay Eye Assoc. Warwick Rhode Island 02888
Zillan Clinical Research Houston Texas 77082
Hoopes Vision Draper Utah 84020

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 NCT07140783, 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 21, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07140783 live on ClinicalTrials.gov.

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