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Clinical Trials in the USA / NCT07557030
Starting soon Not applicable

Optimization for Toric Contact Lenses

NCT07557030 · tracked via the Priya Life Science USA tracker
Sponsor
CooperVision International Limited (CVIL)
Phase
Not applicable
Started
2026-05
Last updated
2026-05-06

Condition(s) studied

AstigmatismAmetropia

Investigational drug(s) / intervention(s)

Lens 1 ( stenfilcon A )Lens 2 ( comfilcon A )

Lens 1 ( stenfilcon A ): 15 minutes of daily wear

Lens 2 ( comfilcon A ): 15 minutes of daily wear

Study summary

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

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. They are at least 18 years of age. 2. They understand their rights as a research participant and are willing and able to sign a Statement of Informed Consent. 3. They have spherical refractive error at the corneal plane between +4.00 to -7.00DS 4. They have refractive astigmatism at the corneal plane of 0.75 to 2.25DC in one eye. 5. They are able to achieve distance HCHL visual acuity of +0.10 logMAR or better in each eye 6. 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: 1. Is participating in any concurrent clinical or research trial. 2. They have an ocular disorder which would normally contra-indicate contact lens wear. 3. They have a systemic disorder which would normally contra-indicate contact lens wear. 4. They are pseudophakic or aphakic. 5. They have had corneal refractive surgery. 6. They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus. 7. Is using any systemic or topical medications that in the opinion of the investigator may affect contact lens wear or a study outcome variable.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Indiana University Bloomington Indiana

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07557030 on ClinicalTrials.gov ↗ ← All trials in the USA