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Clinical Trials/NCT00799422
NCT00799422
Completed
Not Applicable

Evaluation of Lens Fit, Lens Parameters, and Circumlimbal Conjunctival Staining (CSS) in Normal Patients

Alcon Research1 site in 1 country26 target enrollmentNovember 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Conjunctival Staining
Sponsor
Alcon Research
Enrollment
26
Locations
1
Primary Endpoint
Mean Circumlimbal Conjunctival Staining Score
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

The purpose of this study was to investigate contact lens fit, lens parameters, and conjunctival staining in a sample of subjects with various contact lens/solution combinations.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
March 2009
Last Updated
13 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Successfully wearing hydrogel and/or silicone hydrogel contact lenses;
  • Read, sign, and date informed consent/HIPAA document;
  • Vision correctable to 20/30 (Snellen) or better in each eye at distance with habitual spectacles;
  • Willing and able to discontinue contact lens wear when requested during the study;
  • Other protocol-defined inclusion criteria may apply.

Exclusion Criteria

  • Evidence or history of ocular disease or pathology;
  • One functional eye or a monofit lens;
  • Use of concomitant topical ocular prescription or over-the-counter 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.

Outcomes

Primary Outcomes

Mean Circumlimbal Conjunctival Staining Score

Time Frame: 1 week

Circumlimbal conjunctival staining was expressed as the sum of the individual scores observed across all of the evaluated regions of the eye. The bulbar conjunctiva was assessed by the investigator utilizing a slit-lamp and lissamine green ophthalmic dye. Staining coverage was scored separately in each of four regions (nasal, temporal, inferior, and superior) using a 4-point clinical grading scale (grade 0-3), where Grade 0 = No staining present; Grade 1 = Slight staining present; Grade 2 = Moderate staining present; and Grade 3 = Dense staining present. The scores for the four regions were summed, with a sum score range of 0-12. A lower score represents a more desirable outcome.

Secondary Outcomes

  • Mean Change From Dispense (Day 0) in Lens Base Curve at 1 Week(Dispense (Day 0), 1 week)
  • Mean Change From Dispense (Day 0) in Lens Diameter at 1 Week(Dispense (Day 0), 1 week)

Study Sites (1)

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