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Clinical Trials/NCT00713076
NCT00713076CompletedNot Applicable

Wettability of Contact Lenses With a Multi-Purpose Solution

Alcon Research2 sites in 1 country30 target enrollmentStarted: October 2007Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
2
Primary Endpoint
Lens Wettability - ex-vivo wetting angle
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Measure wettability of hydrogel and silicone hydrogel contact lenses presoaked in a Multi-Purpose Solution.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Subjects with normal eyes who have successfully worn contact lenses on a daily basis for at least two weeks prior to the study.
  • •Must be wearing lenses a minimum of eight hours a day
  • •Vision must be correctable to 20/30 (snellen) or better in each eye at a distance with soft contact lenses
  • •Use no topical ocular OTC or prescribed ocular medication

Exclusion Criteria

  • •Subjects with current lid or conjunctival infections, abnormalities, inflammation, abnormal corneal opacities, significant lenticular inclusions, iritis, ocular disease or condition, corneal surgery, cataract surgery, intraocular lens implants, or glaucoma filtering surgery.
  • •Subjects using systemic medications, upper respiratory infections or colds, history of seasonal allergies with significant ocular side effects

Outcomes

Primary Outcomes

Lens Wettability - ex-vivo wetting angle

Time Frame: From baseline

Secondary Outcomes

  • Slit-lamp findings Corrected visual acuity (snellen) Adverse events(From baseline)

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (2)

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