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Comfort and Cleaning Evaluation of Multipurpose Solutions in Contact Lens Patients

This study has been completed.
Sponsor:
Information provided by:
Innovative Medical
ClinicalTrials.gov Identifier:
NCT00519948
First received: August 21, 2007
Last updated: June 16, 2008
Last verified: June 2008
  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: 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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: 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

No publications provided

Responsible Party: Dr. Chu, Eyeworks Group
ClinicalTrials.gov Identifier: NCT00519948     History of Changes
Other Study ID Numbers: 5320
Study First Received: August 21, 2007
Last Updated: June 16, 2008
Health Authority: United States: Institutional Review Board

ClinicalTrials.gov processed this record on November 20, 2014