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Assessing Ocular Surface Changes After Changing Glaucoma Medications

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ClinicalTrials.gov Identifier: NCT00554411
Recruitment Status : Completed
First Posted : November 6, 2007
Last Update Posted : January 27, 2017
Sponsor:
Information provided by (Responsible Party):

Study Description
Brief Summary:
Hypothesis: Changing to Travatan Z therapy increases the tear film break up time of subjects on Xalatan therapy presenting with ocular surface disease.

Condition or disease
Glaucoma Monotherapy With Xalatan From 1 to 18 Months Ocular Surface Disease

Detailed Description:
Patients who have been taking Xalatan monotherapy to treat their glaucoma and presenting with ocular surface disease will be advised to switch their medication to Travatan Z. Test results will be recorded at the day that the medication was changed and at follow-up to determine if there is a measurable change in tear film break up, corneal staining and in the Ocular Surface Disease Index.

Study Design

Study Type : Observational
Actual Enrollment : 22 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Assessing Changes at the Ocular Surface Following the Switch From Xalatan to Travatan Z.
Study Start Date : November 2007
Primary Completion Date : August 2011
Study Completion Date : August 2011

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Eye Care Glaucoma
U.S. FDA Resources

Groups and Cohorts


Outcome Measures

Primary Outcome Measures :
  1. Change in Signs and Symptoms of Ocular Surface Disease [ Time Frame: 6 months ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients will be selected from the ophthalmology clinic of the principal investigator
Criteria

Inclusion Criteria:

  • on Xalatan monotherapy from 1 to 18 months
  • 18 years of age or older
  • has been diagnosed with ocular surface disease

Exclusion Criteria:

  • special populations such as children, pregnant females, prisoners, etc.
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00554411


Locations
United States, Colorado
Rocky Mountain Lions Eye Institute
Aurora, Colorado, United States, 80045-0510
Sponsors and Collaborators
University of Colorado, Denver
Investigators
Principal Investigator: Malik Y Kahook, M.D. Rocky mountain Lions Eye Institute
More Information

Responsible Party: University of Colorado, Denver
ClinicalTrials.gov Identifier: NCT00554411     History of Changes
Other Study ID Numbers: 07-0757
First Posted: November 6, 2007    Key Record Dates
Last Update Posted: January 27, 2017
Last Verified: January 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by University of Colorado, Denver:
Travatan Z
glaucoma
tear film break up time

Additional relevant MeSH terms:
Glaucoma
Ocular Hypertension
Eye Diseases
Travoprost
Antihypertensive Agents