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Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00483795
First Posted: June 7, 2007
Last Update Posted: July 25, 2007
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
June 1, 2007
June 7, 2007
July 25, 2007
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Complete list of historical versions of study NCT00483795 on ClinicalTrials.gov Archive Site
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Pilot Evaluation of Two Multipurpose Solutions in Regards to Corneal Staining
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To evaluate corneal staining after contact lens instillation with two different multi purpose solutions.
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Interventional
Phase 4
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single
Corneal Staining
Drug: sodium citrate, sodium chloride, sodium borate, propylene glycol. citrate, tetronic 1304, AMP 95
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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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
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
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Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00483795
5308
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Innovative Medical
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Principal Investigator: Thomas Kislan, OD Hazleton Eye Specialists
Innovative Medical
July 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP