A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma
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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. |
ClinicalTrials.gov Identifier: NCT00051181 |
Recruitment Status :
Completed
First Posted : January 7, 2003
Last Update Posted : August 5, 2008
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Glaucoma, Angle-Closure Ocular Hypertension | Drug: Travoprost (0.004%) Drug: Latanoprost (0.005%) | Phase 3 |
Study Type : | Interventional (Clinical Trial) |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Double |
Primary Purpose: | Treatment |
Official Title: | A Safety and Efficacy Study of Travoprost 0.004% Compared to Latanoprost 0.005% in Patients With Chronic Angle-Closure Glaucoma. |
Study Start Date : | January 2000 |
Actual Primary Completion Date : | June 2003 |
Actual Study Completion Date : | June 2003 |

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |

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): NCT00051181
United States, Texas | |
Asia | |
Fort Worth, Texas, United States | |
Australia | |
Australia | |
Sidney, Australia |
ClinicalTrials.gov Identifier: | NCT00051181 |
Other Study ID Numbers: |
C-01-38 |
First Posted: | January 7, 2003 Key Record Dates |
Last Update Posted: | August 5, 2008 |
Last Verified: | August 2008 |
Glaucoma POAG OAG OHT |
Glaucoma Ocular Hypertension Glaucoma, Angle-Closure Eye Diseases |
Latanoprost Travoprost Antihypertensive Agents |