Status:

COMPLETED

Three Month Clinical Evaluation of the Contamac 74% Silicone Hydrogel Contact Lens

Lead Sponsor:

Contamac Ltd

Conditions:

Vision Correction

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to compare the clinical performance of the contamac silicone hydrogel contact lens with a predicate device (Cooper Vision Biofinity).

Detailed Description

The purpose of this study is to evaluate the clinical performance of the Contamac lens in comparison with a currently marketed silicone hydrogel: Biofinity® (CooperVision). This is a 3-month, open-lab...

Eligibility Criteria

Inclusion

  • existing contact lens wearer
  • read and signed statement of informed consent
  • has clear central cornea
  • requires spherical distance correction

Exclusion

  • has worn RGP contact lenses within the last 30 days
  • is using any ocular medication
  • has had refractive surgery
  • has an infectious disease
  • is pregnant or lactating
  • is participating in another clinical research study

Key Trial Info

Start Date :

August 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

February 1 2009

Estimated Enrollment :

57 Patients enrolled

Trial Details

Trial ID

NCT01197859

Start Date

August 1 2008

End Date

February 1 2009

Last Update

August 12 2020

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Vision Care Research

Farnham, Surry, United Kingdom, GU9 7EN

Three Month Clinical Evaluation of the Contamac 74% Silicone Hydrogel Contact Lens | DecenTrialz