Status:

COMPLETED

The Clinical Evaluation of Two Daily Disposable Contact Lenses

Lead Sponsor:

Johnson & Johnson Vision Care, Inc.

Collaborating Sponsors:

Eurolens Research

Conditions:

Myopia

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The objective of this study is to evaluate the clinical performance of two daily disposable contact lenses.

Eligibility Criteria

Inclusion

  • They are of legal age (18 years) and capacity to volunteer.
  • They understand their rights as a research subject and are willing to sign a Statement of Informed Consent.
  • They are willing and able to follow the protocol.
  • They would be expected to attain at least 6.9 (20/30) in each eye with the study lenses.
  • They are able to wear contact lenses which have a back vertex power of -1.00 to -6.00DS.
  • They have a maximum of 1.00D of refractive astigmatism (i.e. \< 1.00 DC).
  • They have worn soft contact lenses within six months of starting the study.

Exclusion

  • 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 has keratoconus.
  • They are pregnant or lactating.
  • They have grade 2 or greater of any of the following ocular surface signs: corneal edema, corneal vascularization, corneal staining, tarsal conjunctival changes or any other abnormality which would normally contraindicate contact lens wear.
  • They have any infectious disease (e.g., hepatitis) or any immunosuppressive disease (e.g., HIV).
  • They have diabetes.
  • They are currently taking part in any other clinical study or research.

Key Trial Info

Start Date :

August 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2007

Estimated Enrollment :

65 Patients enrolled

Trial Details

Trial ID

NCT00762996

Start Date

August 1 2007

End Date

October 1 2007

Last Update

June 19 2018

Active Locations (1)

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Eurolens Research

Manchester, United Kingdom, M60 1QD