Phentolamine Ophthalmic Solution for Night Vision After Eye Surgery

This study is testing Phentolamine Ophthalmic Solution to see if it can improve vision in low light (mesopic visual acuity) for adults who have had keratorefractive surgery (like LASIK or PRK). Researchers also want to understand how safe Phentolamine Ophthalmic Solution is. You might be able to join if you are 18 or older, have had eye surgery more than 6 months ago, and experience night vision problems like glare or halos. The study will compare Phentolamine Ophthalmic Solution to a placebo (a drop with no medicine) to see if it improves your vision by at least 3 lines on an eye chart after 15 days. The study aims to enroll 200 participants, but its current status is unclear.

Study design
This is a randomized, placebo-controlled, and double-masked study, meaning neither you nor your doctor will know if you are receiving Phentolamine Ophthalmic Solution or the placebo. It plans to include 200 participants.
What's involved
You would use Phentolamine Ophthalmic Solution or a placebo drop once daily for 2 weeks. You would also visit the clinic once a week for 2 weeks for checkups and tests, and keep a daily diary of when you use the drops.
Compensation
Not stated in the trial record.
Follow-up
Your vision will be measured at Day 15, which is the primary endpoint for the study.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07140783

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

Recruiting
PHASE3Ages 18+InterventionalTreatment
Ocuphire Pharma, Inc.
~580 participants
Updated 2026-09-08 on ClinicalTrials.gov
What's tested:0.75% Phentolamine Ophthalmic SolutionPlacebo

At a glance

Recruiting sites
20 of 20 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percent of participants with >= 15 ETDRS letters (>= 3 lines) improvement in the study eye in mLCVA compared to Baseline (Day1 pre-dose) at Day 15
Measured over Day 15
Vision Loss Night
Vision Disorders

NCT07140783

Where you'd take part

This study runs at 20 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.

  • Arizona Eye Care

    Chandler, Arizonastudy coordinator listed

    Recruiting

  • California Eye Specialists Medical Group

    Pasadena, Californiastudy coordinator listed

    Recruiting

  • Eye Doctors of Arizona

    Phoenix, Arizonastudy coordinator listed

    Recruiting

  • Eye Research Foundation

    Newport Beach, Californiastudy coordinator listed

    Recruiting

  • Global Research Management

    Glendale, Californiastudy coordinator listed

    Recruiting

  • Gordon Schanzlin New Vision

    La Jolla, Californiastudy coordinator listed

    Recruiting

  • Hoopes Vision

    Draper, Utahstudy coordinator listed

    Recruiting

  • Kannarr Eye Care

    Pittsburg, Kansasstudy coordinator listed

    Recruiting

Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.

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  • Percent of participants with >= 15 ETDRS letters (>= 3 lines) improvement in the study eye in mLCVA compared to Baseline (Day1 pre-dose) at Day 15Day 15

    To evaluate the efficacy of POS to improve mLCVA in subjects with previous keratorefractive surgery