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Upneeq vs. Lumify Ptosis

StatusNot Yet Recruiting
PhasePhase 4
Started2026-12-01
View on ClinicalTrials.gov ↗

Amendment history

2026-05-20
critical
Study Status v1
Primary completion pushed: 2026-08-01 → 2027-08-01
Completion pushed: 2026-12-01 → 2027-12-01
Start date2026-03-01→2026-12-01
2026-01-29
minor
Original filing
455 trials monitored
See 53 trials at risk
This study aims to compare the short-term effect of oxymetazoline 0.1% (Upneeq) versus brimonidine 0.025% (Lumify) on upper-eyelid position in adults with acquired ptosis. Participants will undergo standardized eyelid photography, receive a single dose of either Upneeq or Lumify in randomized order, and have repeat photographs approximately 60 minutes later. They will return for a second visit to receive the alternate medication using the same procedures. Eyelid height measurements will be obtained from coded images by masked graders. Data will be analyzed using paired statistical methods appropriate for a crossover design. Both medications are FDA-approved topical ophthalmic drops, and the study involves minimal risk with anticipated transient ocular irritation as the most common adverse event.
Trial Details
NCT Number NCT07390578
Lead Sponsor Duke University
Conditions Acquired Ptosis
Enrollment 50 participants
Start Date 2026-12-01
Primary Completion 2027-08-01 (estimated)
Study Completion 2027-12-01 (estimated)
Updated on ClinicalTrials.gov 2026-05-22