Optimization for Toric Contact Lenses

Part of paid clinical trials in Bloomington, Indiana.

Sponsor
CooperVision International Limited (CVIL)
Study ID
NCT07557030
Status
Not Yet Recruiting

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Conditions

  • Ametropia
  • Astigmatism

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Lens 1 ( stenfilcon A ) — DEVICE
    15 minutes of daily wear
  • Lens 2 ( comfilcon A ) — DEVICE
    15 minutes of daily wear

Study Details

The aim of this study is to evaluate the agreement between subjective and objective toric lens prescriptions.

Key Dates

Start date
May 31, 2026
Status verified
May 2026
Primary completion
Aug 31, 2026
Completion
Aug 31, 2026

Study Design

Enrollment
45 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Lens 1 ( stenfilcon A)
    All participants will be randomized to wear lens A
  • Experimental: Lens 2 ( comfilcon A)
    All participants will be randomized to wear lens B

Primary Outcome Measure

Subjective assessment of optimization of Toric lenses [ Time Frame: At the End of Baseline 15 minutes of daily wear ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Indiana UniversityBloomingtonIndiana47405-

Find similar trials in Bloomington, IN

By research site
Indiana University· Bloomington, IN

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