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Study identifier: NCT07650708 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Multicenter, Open-Label Study to Evaluate Perioperative Treatment of Dry Eye With Miebo® in Subjects Undergoing LASIK

Condition: Dry Eye Syndrome (DES) · Dry Eye Disease (DED)  ·  Sponsor: Vance Thompson Vision

PhasePhase 4
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Compare eye dryness following laser-assisted in situ keratomileusis (LASIK) surgery to eye dryness prior to receiving perioperative Miebo in patients with dry eye disease (DED)

This description comes directly from the study's public registry record.

Talk to the study team

Kayla Karpuk, OD  ·  605-371-6883  ·  kayla.karpuk@vancethompsonvision.com

Always discuss trial participation with your own doctor first.

Locations (4)

Vance Thompson Vision- BozemanBozeman, Montana, United StatesRecruiting
Vance Thompson Vision- OmahaOmaha, Nebraska, United StatesNot Yet Recruiting
Vance Thompson Vision- FargoFargo, North Dakota, United StatesRecruiting
Vance Thompson Vision- Sioux FallsSioux Falls, South Dakota, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07650708