CompletedNot Applicable

A Clinical Comparison of Two Soft Contact Lenses (C24-755)

United Kingdom52 participantsStarted 2024-11-18

Plain-language summary

The aim of this study is to compare the short-term clinical performance of two soft contact lenses.

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✓. They are of legal age (18) and capacity to volunteer.
✓. They understand their rights as a research subject and are willing and able to sign a Statement of Informed Consent.
✓. They are willing and able to follow the protocol.
✓. They currently wear soft contact lenses, or have done so within the past two years.
✓. They are expected to be able to be fitted with the study lenses within the power range available.

✕. 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 using any topical medication such as eye drops or ointment.
✕. They are aphakic.
✕. They have had corneal refractive surgery.
✕. They have any corneal distortion resulting from previous hard or rigid lens wear or have keratoconus.
✕. They are pregnant or breastfeeding.
✕. They have an eye or health condition including an immunosuppressive or infectious disease which would, in the opinion of the investigator, contraindicate contact lens wear or pose a risk to study personnel; or a history of anaphylaxis or severe allergic reaction.

Subjective Overall Score

Timeframe: At the end of 15 minutes of daily wear

NCT IDNCT06758076

SponsorCooperVision, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2025-01-31