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NCT Number: NCT07557030

Optimization for Toric Contact Lenses

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

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Indiana University

Bloomington, Indiana, 47405, United States

About this study

To evaluate agreement between subjective and objective optimized toric contact lens prescriptions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • They are at least 18 years of age.
  • They understand their rights as a research participant and are willing and able to sign a Statement of Informed Consent.
  • They have spherical refractive error at the corneal plane between +4.00 to -7.00DS
  • They have refractive astigmatism at the corneal plane of 0.75 to 2.25DC in one eye.
  • They are able to achieve distance HCHL visual acuity of +0.10 logMAR or better in each eye
  • They are a current soft contact lens wearer or have previous experience of successful soft contact lens wear in the past 3 years.

Exclusion criteria

  • Is participating in any concurrent clinical or research trial.
  • They have an ocular disorder which would normally contra-indicate contact lens wear.
  • They have a systemic disorder which would normally contra-indicate contact lens wear.
  • They are pseudophakic or aphakic.
  • They have had corneal refractive surgery.
  • They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.
  • Is using any systemic or topical medications that in the opinion of the investigator may affect contact lens wear or a study outcome variable.

Treatment and study plan

Lens 1 ( stenfilcon A )

Device

15 minutes of daily wear

Lens 2 ( comfilcon A )

Device

15 minutes of daily wear

Primary outcomes

  1. Subjective assessment of optimization of Toric lenses

    Time frame: At the End of Baseline 15 minutes of daily wear

    Proportion of eyes in which the optimized toric lens cylinder axis determined by the subjective method agrees with that determined by the objective method within ±10 degrees (measured at a single time point).

Study contacts

Contact information is provided by the study sponsor or research team.

Kelly Voltz

CONTACT

[email protected]

+19256604364

Sponsors and collaborators

Lead sponsor

CooperVision International Limited (CVIL)

Industry

Collaborators

  • Indiana University

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Apr 29, 2026
Registry last updated
May 6, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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