Assessing Ocular Surface Changes After Changing Glaucoma Medications
This study has been completed.
Sponsor:
University of Colorado, Denver
Information provided by (Responsible Party):
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT00554411
First received: November 2, 2007
Last updated: January 29, 2013
Last verified: January 2013
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Purpose
hypothesis: changing to Travatan Z therapy increases the tear film break up time of subjects on Xalatan therapy presenting with ocular surface disease.
| Condition |
|---|
|
Glaucoma Monotherapy With Xalatan From 1 to 18 Months Ocular Surface Disease |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Assessing Changes at the Ocular Surface Following the Switch From Xalatan to Travatan Z. |
Resource links provided by NLM:
Genetics Home Reference related topics:
early-onset glaucoma
MedlinePlus related topics:
Glaucoma
Drug Information available for:
Travoprost
U.S. FDA Resources
Further study details as provided by University of Colorado, Denver:
Primary Outcome Measures:
- Change in Signs and Symptoms of Ocular Surface Disease [ Time Frame: 6 months ] [ Designated as safety issue: No ]
| Enrollment: | 22 |
| Study Start Date: | November 2007 |
| Study Completion Date: | August 2011 |
| Primary Completion Date: | August 2011 (Final data collection date for primary outcome measure) |
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 record 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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| 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 t 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
Please refer to this study by its ClinicalTrials.gov identifier: 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
No publications provided
| Responsible Party: | University of Colorado, Denver |
| ClinicalTrials.gov Identifier: | NCT00554411 History of Changes |
| Other Study ID Numbers: | 07-0757 |
| Study First Received: | November 2, 2007 |
| Last Updated: | January 29, 2013 |
| Health Authority: | United States: Institutional Review Board |
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 Cardiovascular Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 23, 2013