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Comfort and Cleaning Evaluation of Multipurpose Solutions in Contact Lens Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00519948
First Posted: August 23, 2007
Last Update Posted: June 19, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Innovative Medical
  Purpose
To compare patient comfort and overall lens cleanliness with consecutive use of two multipurpose lens solutions.

Condition Intervention Phase
Patient Comfort Lens Cleanliness Drug: new MPS, opti-free express no rub MPS Phase 4

Study Type: Interventional
Study Design: Intervention Model: Crossover Assignment
Masking: None (Open Label)

Further study details as provided by Innovative Medical:

Enrollment: 20
Study Completion Date: June 2008
Primary Completion Date: June 2008 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Criteria

Inclusion Criteria:

  1. Patients 18 yrs or older
  2. Males or females
  3. Any race or ethnic background
  4. CL patients using Opti-Free Express no-rub MPS currently
  5. Patients using Focus night and day Lenses

Exclusion Criteria:

  1. Corneal refractive surgery within 6 months of this study.
  2. Corneal ectasia.
  3. Current use of Restasis
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00519948


Locations
United States, Texas
Eyeworks Group
Fort Worth, Texas, United States, 76132
Sponsors and Collaborators
Innovative Medical
Investigators
Principal Investigator: Robert Chu, OD Eyeworks Group
  More Information

Responsible Party: Dr. Chu, Eyeworks Group
ClinicalTrials.gov Identifier: NCT00519948     History of Changes
Other Study ID Numbers: 5320
First Submitted: August 21, 2007
First Posted: August 23, 2007
Last Update Posted: June 19, 2008
Last Verified: June 2008


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