Evaluation of Mesopic Visual Acuity and Patient Satisfaction Following Ray-Tracing-Guided LASIK

Part of paid clinical trials in Sioux Falls, South Dakota.

Sponsor
Vance Thompson Vision
Study ID
NCT07790185
Phase
PHASE4
Status
Recruiting

Conditions

  • Astigmatism
  • Myopia

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Not accepted

Interventions

  • Wavelight Plus — DEVICE
    comprehensive evaluation of WaveLight® Plus technology by assessing impact on both functional low-light vision and patient reported outcomes

Study Details

To provide comprehensive evaluation of WaveLight® Plus technology by assessing impact on both functional low-light vision and patient reported outcomes

Key Dates

First listed
Aug 27, 2026
Start date
Apr 20, 2026
Status verified
Aug 2026
Primary completion
Sep 30, 2027
Completion
Nov 30, 2027

Study Design

Enrollment
50 participants (estimated)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE

Arms

  • Experimental: WaveLight Plus

Primary Outcome Measure

Establish non-inferiority of the post-operative uncorrected mesopic distance visual acuity MVA (UC-MVA, monocular) at 6 months to the pre-operative Best Spectacle-Corrected MVA (BSC-MVA, monocular), assessed in logMAR units [ Time Frame: Baseline compared to 6 month post operative visit ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Vance Thompson VisionSioux FallsSouth Dakota57108
Kayla Karpuk, OD
605-361-3937

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