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Comparison of OPTI-FREE RepleniSH and ReNu Multi-Plus Lens Care Regimens on Corneal Epithelium

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Alcon

Status

Completed

Conditions

Contact Lens Wear

Treatments

Device: OPTI-FREE RepleniSH
Device: ReNu MultiPlus MPS

Study type

Interventional

Funder types

Industry

Identifiers

NCT00724269
SMA-08-04 / BP-08-01

Details and patient eligibility

About

The purpose of this study is to evaluate the corneal epithelium after soft contact lens wear and use of two marketed multi-purpose solutions.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Successful contact lens wear on a daily wear basis
  • Wear contact lenses at least 8 hours/day
  • Vision correctable to at least 20/30
  • Normal Eyes
  • Other protocol-defined inclusion criteria may apply

Exclusion:

  • Topical ocular medication use
  • Other protocol-defined inclusion criteria may apply

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

20 participants in 2 patient groups

Opti Free RepliniSH
Active Comparator group
Description:
Opti Free RepliniSH
Treatment:
Device: OPTI-FREE RepleniSH
ReNu Multi-Plus
Active Comparator group
Description:
ReNu Multi-Plus
Treatment:
Device: ReNu MultiPlus MPS

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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