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Evaluation of Deposits on Contact Lenses Worn Daily Wear

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Alcon

Status

Completed

Conditions

Refractive Error

Treatments

Device: Balafilcon A contact lenses (PureVision)
Device: Etafilcon A contact lenses (Acuvue2)

Study type

Interventional

Funder types

Industry

Identifiers

Details and patient eligibility

About

The purpose of this study was to measure front surface deposits on contact lenses when worn for ten hours.

Enrollment

55 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older.
  • Visual acuity correctable to 20/30 (Snellen) or better in each eye at distance with contact lenses.
  • Successfully wearing hydrogel or silicone hydrogel contact lenses prior to enrollment in the study.
  • Other protocol-defined inclusion criteria may apply.

Exclusion criteria

  • Evidence or history of keratitis (dendritic keratitis); viral disease of the cornea and/or conjunctiva; acute bacterial disease of the cornea and/or conjunctiva and/or eyelids; infection of the eye; and/or fungal disease of the eye.
  • One functional eye or a monofit lens.
  • Ocular conditions such as active acute blepharitis, conjunctival infections, and iritis.
  • Any slit-lamp finding score of (1) at the Screening Visit as defined in protocol.
  • Use of concomitant topical ocular prescription or over-the-counter (OTC) ocular medications.
  • History of seasonal allergies with significant ocular side effects which may have an adverse impact on contact lens wear.
  • Other protocol-defined exclusion criteria may apply.

Trial design

55 participants in 2 patient groups

PureVision/Acuvue 2
Other group
Description:
PureVision contact lenses worn first, with Acuvue 2 contact lenses worn second. Both products worn for 10 hours each.
Treatment:
Device: Etafilcon A contact lenses (Acuvue2)
Device: Balafilcon A contact lenses (PureVision)
Acuvue 2/PureVision
Other group
Description:
Acuvue 2 contact lenses worn first, with PureVision contact lenses worn second. Both products worn for 10 hours each.
Treatment:
Device: Etafilcon A contact lenses (Acuvue2)
Device: Balafilcon A contact lenses (PureVision)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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