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.
OPI-NXYDLD-303 Safety and Efficacy of Phentolamine Ophthalmic Solution in Keratorefractive Surgery Participants With Decreased Mesopic Visual Acuity
At a glance
Conditions
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.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- 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