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Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining
This study has been completed.
Sponsored by: Innovative Medical
Information provided by: Innovative Medical
ClinicalTrials.gov Identifier: NCT00483795
  Purpose

To evaluate corneal staining after contact lens instillation with two different multi purpose solutions.


Condition Intervention Phase
Corneal Staining
Drug: sodium citrate, sodium chloride, sodium borate, propylene glycol. citrate, tetronic 1304, AMP 95
Phase IV

MedlinePlus related topics: Dietary Sodium
Drug Information available for: Propylene glycol Sodium chloride Citric acid Sodium Citrate Chlorides Sodium borate
U.S. FDA Resources
Study Type: Interventional
Study Design: Randomized, Single Blind, Active Control, Parallel Assignment
  Eligibility

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

Inclusion Criteria:

  • Patients 18 yrs or older
  • Males or females
  • Any race or ethnic background
  • CL patients using (multipurpose solutions) MPS
  • Patients using Acuvue 2 lenses

Exclusion Criteria:

  • Corneal refractive surgery within 6 months of this study.
  • Contact lens use on day of examination.
  • Corneal ectasia.
  • Current use of Restasis
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00483795

Locations
United States, Pennsylvania
Hazleton Eye Specialists
Hazleton, Pennsylvania, United States, 18202
Sponsors and Collaborators
Innovative Medical
Investigators
Principal Investigator: Thomas Kislan, OD Hazleton Eye Specialists
  More Information

Study ID Numbers: 5308
Study First Received: June 1, 2007
Last Updated: July 23, 2007
ClinicalTrials.gov Identifier: NCT00483795  
Health Authority: United States: Institutional Review Board

Study placed in the following topic categories:
Citric Acid

ClinicalTrials.gov processed this record on January 14, 2009