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Sponsored by: |
Alcon Research |
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Information provided by: | Alcon Research |
ClinicalTrials.gov Identifier: | NCT00708422 |
The objective of this study is to examine the affect on tear film break up time (TBUT) of changing patients on Xalatan® therapy to TRAVATAN Z®.
Condition | Intervention | Phase |
---|---|---|
Glaucoma |
Drug: Travoprost eye drop Drug: Latanoprost |
Phase IV |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Outcomes Assessor), Parallel Assignment |
Estimated Enrollment: | 110 |
Study Start Date: | July 2008 |
Estimated Primary Completion Date: | January 2009 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1: Active Comparator
Travoprost BAK-free
|
Drug: Travoprost eye drop
Ophthalmic solution
|
2: Active Comparator
Latanoprost
|
Drug: Latanoprost |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Alcon ( Mark Jasek ) |
Study ID Numbers: | SMA-08-07 |
Study First Received: | June 30, 2008 |
Last Updated: | July 1, 2008 |
ClinicalTrials.gov Identifier: | NCT00708422 |
Health Authority: | United States: Food and Drug Administration |
Glaucoma TBUT IOP |
Glaucoma Eye Diseases Tetrahydrozoline Latanoprost |
Travoprost Hypertension Ocular Hypertension |
Therapeutic Uses Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions |