Comfort Evaluation of a New MPS vs. Replenish in Contact Lens Patients

This study has been completed.
Information provided by:
Innovative Medical Identifier:
First received: August 17, 2007
Last updated: April 21, 2008
Last verified: April 2008
To compare corneal staining after contact lens instillation with a new MPS vs. RepleniSH

Condition Intervention Phase
Corneal Staining
Other: new MPS
Other: RepleniSH
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single Blind (Investigator)

Resource links provided by NLM:

Further study details as provided by Innovative Medical:

Enrollment: 24
Study Completion Date: April 2008
Primary Completion Date: April 2008 (Final data collection date for primary outcome measure)

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both

Inclusion Criteria:

  1. Patients 18 yrs or older
  2. Males or females
  3. Any race or ethnic background
  4. CL patients using MPS products currently
  5. Patients using Contact Lenses habitually (at least 1 month)

Exclusion Criteria:

  1. Corneal refractive surgery within 6 months of this study.
  2. Contact lens use on day of examination.
  3. Corneal ectasia.
  4. 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 identifier: NCT00518700

United States, California
Private Practice
Azusa, California, United States, 91702
Sponsors and Collaborators
Innovative Medical
Principal Investigator: Milton Hom, OD, FAAO Private Practice
  More Information

No publications provided

Responsible Party: Innovative medical, Innovative Medical Identifier: NCT00518700     History of Changes
Other Study ID Numbers: 5321
Study First Received: August 17, 2007
Last Updated: April 21, 2008
Health Authority: United States: Institutional Review Board processed this record on December 01, 2015