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Cross-Over Evaluation of Two Lubricating Eye Drops

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00493662
First Posted: June 28, 2007
Last Update Posted: January 15, 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
June 26, 2007
June 28, 2007
January 15, 2008
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Complete list of historical versions of study NCT00493662 on ClinicalTrials.gov Archive Site
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Cross-Over Evaluation of Two Lubricating Eye Drops
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To evaluate the efficacy of two lubricating eye drops for the treatment of dry eye signs and symptoms.
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Interventional
Phase 4
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Single
Dry Eye
  • Drug: Polyethylene Glycol 400 0.4%
  • Drug: Propylene Glycol 0.3%
  • Drug: 0.15% sodium Hyaluronate
  • Drug: sodium chloride
  • Drug: sodium phosphate monobasic
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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:

  1. Patients 18 yrs or older
  2. Males or females
  3. Any race or ethnic background
  4. Patients with present ocular surface discomfort and a SESoD score of at least 2

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
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
 
 
NCT00493662
5310
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Innovative Medical
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Principal Investigator: Tom Kislan, OD Hazleton Eye Specialists
Innovative Medical
January 2008

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